X-46332445-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332445
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332445
    reference: chr 0
allele count: 1
allele frequency: 1.270664176164881e-5
allele num: 78699
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.499T>C
  hgvsp: ENSP00000298190.6:p.Ter167ArgextTer3
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*258T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9717T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.514T>C
  hgvsp: ENSP00000345797.4:p.Ter172ArgextTer3
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*261T>C
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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 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
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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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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 589
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
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  variant carriers: 0
hgvs: p.Ter172ArgextTer3
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

X-46332451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332451
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332451
    reference: chr 0
allele count: 5
allele frequency: 6.392145331816264e-5
allele num: 78221
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*4A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*4A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9723A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*264A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*267A>G
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  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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  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: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 170
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2255
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

X-46332457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332457
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332457
    reference: chr 0
allele count: 1
allele frequency: 1.283861856464244e-5
allele num: 77890
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*10A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9729A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*10A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*270A>G
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*273A>G
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-46332474-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332474
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332474
    reference: chr 0
allele count: 2
allele frequency: 2.596728122565568e-5
allele num: 77020
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*27G>T
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*287G>T
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9746G>T
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*27G>T
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*290G>T
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
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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
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1295
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  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

X-46332476-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332476
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332476
    reference: chr 0
allele count: 3
allele frequency: 3.893676669089399e-5
allele num: 77048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*289T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*29T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9748T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*292T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*29T>C
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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 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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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 248
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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
  all individuals: 5663
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-46332486-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332486
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332486
    reference: chr 0
allele count: 2
allele frequency: 2.618726513296584e-5
allele num: 76373
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*299A>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*39A>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*39A>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*302A>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9758A>C
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  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 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
  all individuals: 3873
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

X-46332497-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332497
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332497
    reference: chr 0
allele count: 4
allele frequency: 5.30968752488916e-5
allele num: 75334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*50G>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*313G>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*50G>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*310G>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9769G>C
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11387
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 9.75e1
  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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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

X-46332499-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046332499
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046332499
    reference: chr 0
allele count: 4
allele frequency: 5.308066934724047e-5
allele num: 75357
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000298190
  ensembl transcript: ENST00000298190
  gene symbol: KRBOX4
  hgvsc: ENST00000298190.6:c.*52T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.238+9771T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418076
  ensembl transcript: ENST00000487081
  gene symbol: KRBOX4
  hgvsc: ENST00000487081.1:c.*312T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000353113
  ensembl transcript: ENST00000360017
  gene symbol: KRBOX4
  hgvsc: ENST00000360017.5:c.*315T>C
  variant of: http://identifiers.org/hgnc/26007
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000345797
  ensembl transcript: ENST00000344302
  gene symbol: KRBOX4
  hgvsc: ENST00000344302.4:c.*52T>C
  variant of: http://identifiers.org/hgnc/26007
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 1212
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-46356530-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046356530
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046356530
    reference: chr 0
allele count: 2
allele frequency: 2.563116749967961e-4
allele num: 7803
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.239-27C>A
  variant of: http://identifiers.org/hgnc/26007
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 158
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population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 83
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-46356583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046356583
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046356583
    reference: chr 0
allele count: 67
allele frequency: 8.202742409402547e-3
allele num: 8168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.265A>G
  hgvsp: ENSP00000418146.1:p.Lys89Glu
  variant of: http://identifiers.org/hgnc/26007
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Lys89Glu
num of homozygotes: 2
population: African
  type: Population
  allele count: 2
  allele frequency: 4.158004158004158e-3
  allele num: 481
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 24
  allele frequency: 5.326231691078562e-3
  allele num: 4506
  num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

X-46356589-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046356589
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046356589
    reference: chr 0
allele count: 1
allele frequency: 1.225340031858841e-4
allele num: 8161
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.271T>C
  hgvsp: ENSP00000418146.1:p.Cys91Arg
  variant of: http://identifiers.org/hgnc/26007
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 3
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  variant carriers: 0
hgvs: p.Cys91Arg
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 160
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2793
  num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

X-46356634-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046356634
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046356633
    reference: chr 0
allele count: 2
allele frequency: 2.48323814253787e-4
allele num: 8054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147121
  ensembl protein: ENSP00000418146
  ensembl transcript: ENST00000478600
  gene symbol: KRBOX4
  hgvsc: ENST00000478600.1:c.*36delA
  variant of: http://identifiers.org/hgnc/26007
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2755
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 1
  allele frequency: 1.162790697674419e-2
  allele num: 86
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 475
  num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: CA
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

X-46359234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359234
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359234
    reference: chr 0
allele count: 1
allele frequency: 4.144734115306503e-5
allele num: 24127
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.*44T>C
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.*44T>C
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 196
  num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-46359248-CTAGTAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359248
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359242
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 25033
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.*24_*29delATACTA
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.*24_*29delATACTA
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  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 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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  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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  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2003
  num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: CTAGTAT
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

X-46359251-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359251
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359251
    reference: chr 0
allele count: 1
allele frequency: 3.961180431768667e-5
allele num: 25245
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.*27C>T
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2010
  num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

X-46359271-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359271
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359271
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 29654
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.*7T>G
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.*7T>G
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2667
  num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD

X-46359273-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359273
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359273
    reference: chr 0
allele count: 1
allele frequency: 3.298588204248581e-5
allele num: 30316
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.*5A>C
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.*5A>C
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 123
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2733
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

X-46359280-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359280
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359280
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 32734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1726T>C
  hgvsp: ENSP00000428248.1:p.Ter576ArgextTer7
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1744T>C
  hgvsp: ENSP00000429148.1:p.Ter582ArgextTer7
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: stop lost
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 1
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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hgvs: p.Ter582ArgextTer7
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 18201
  num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

X-46359292-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359292
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359292
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 38400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1714G>T
  hgvsp: ENSP00000428248.1:p.Asp572Tyr
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1732G>T
  hgvsp: ENSP00000429148.1:p.Asp578Tyr
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asp578Tyr
num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 2479
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

X-46359298-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359298
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359298
    reference: chr 0
allele count: 1
allele frequency: 2.414933951556425e-5
allele num: 41409
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1726A>G
  hgvsp: ENSP00000429148.1:p.Thr576Ala
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1708A>G
  hgvsp: ENSP00000428248.1:p.Thr570Ala
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Thr576Ala
num of homozygotes: 0
population: African
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  allele frequency: 0.0e0
  allele num: 5544
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

X-46359299-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359299
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359299
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 41614
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1725C>A
  hgvsp: ENSP00000429148.1:p.His575Gln
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1707C>A
  hgvsp: ENSP00000428248.1:p.His569Gln
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: AC_Adj0_Filter
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genotype quality: GenotypeQuality
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hgvs: p.His575Gln
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population: African
  type: Population
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  allele frequency: 0.0e0
  allele num: 5543
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-46359317-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359317
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359317
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 47342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1689T>G
  hgvsp: ENSP00000428248.1:p.Ile563Met
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1707T>G
  hgvsp: ENSP00000429148.1:p.Ile569Met
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 125
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Ile569Met
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6017
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

X-46359331-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359331
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359331
    reference: chr 0
allele count: 4
allele frequency: 7.888146088465559e-5
allele num: 50709
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1693A>C
  hgvsp: ENSP00000429148.1:p.Lys565Gln
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1675A>C
  hgvsp: ENSP00000428248.1:p.Lys559Gln
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Lys565Gln
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4526
  num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

X-46359362-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359362
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359362
    reference: chr 0
allele count: 1
allele frequency: 1.73457528924043e-5
allele num: 57651
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1644A>G
  hgvsp: ENST00000414387.2:c.1644A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1662A>G
  hgvsp: ENST00000523374.1:c.1662A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.5e0
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Glu554Glu
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3383
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

X-46359365-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359365
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359365
    reference: chr 0
allele count: 1
allele frequency: 1.715530699421866e-5
allele num: 58291
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1641T>C
  hgvsp: ENST00000414387.2:c.1641T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1659T>C
  hgvsp: ENST00000523374.1:c.1659T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3455
  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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hgvs: p.Tyr553Tyr
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 32727
  num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

X-46359369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359369
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359369
    reference: chr 0
allele count: 1
allele frequency: 1.691846989358282e-5
allele num: 59107
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1637C>T
  hgvsp: ENSP00000428248.1:p.Pro546Leu
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1655C>T
  hgvsp: ENSP00000429148.1:p.Pro552Leu
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.5e0
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Pro552Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3387
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
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site quality: MQ
site quality: DP

X-46359373-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359373
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359373
    reference: chr 0
allele count: 1
allele frequency: 1.669644198821231e-5
allele num: 59893
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1633A>G
  hgvsp: ENSP00000428248.1:p.Lys545Glu
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1651A>G
  hgvsp: ENSP00000429148.1:p.Lys551Glu
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
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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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hgvs: p.Lys551Glu
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6811
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

X-46359388-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359388
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359386
    reference: chr 0
allele count: 1
allele frequency: 1.57890581826794e-5
allele num: 63335
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1616_1617delGA
  hgvsp: ENSP00000428248.1:p.Arg539AsnfsTer9
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1634_1635delGA
  hgvsp: ENSP00000429148.1:p.Arg545AsnfsTer9
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Arg545AsnfsTer9
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 448
  num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: TTC
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

X-46359390-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359390
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359390
    reference: chr 0
allele count: 29
allele frequency: 4.555093065263488e-4
allele num: 63665
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1616G>T
  hgvsp: ENSP00000428248.1:p.Arg539Ile
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1634G>T
  hgvsp: ENSP00000429148.1:p.Arg545Ile
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
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  variant carriers: 4
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Arg545Ile
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7158
  num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

X-46359397-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359397
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359397
    reference: chr 0
allele count: 1
allele frequency: 1.533907014556778e-5
allele num: 65193
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1627C>T
  hgvsp: ENSP00000429148.1:p.His543Tyr
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1609C>T
  hgvsp: ENSP00000428248.1:p.His537Tyr
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.His543Tyr
num of homozygotes: 0
population: East Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 5484
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
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site quality: MQ
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site quality: VQSLOD
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X-46359398-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359398
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359398
    reference: chr 0
allele count: 1
allele frequency: 1.532097441397273e-5
allele num: 65270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1608G>A
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  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1626G>A
  hgvsp: ENST00000523374.1:c.1626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Val542Val
num of homozygotes: 0
population: East Asian
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  allele num: 5485
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population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
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site quality: ClippingRankSum
site quality: FS
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site quality: VQSLOD
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X-46359402-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359402
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359402
    reference: chr 0
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
alternate allele: G
annotation: Annotation
  canonical: true
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  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1622T>C
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  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1604T>C
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  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
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genotype depth: GenotypeDepth
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hgvs: p.Ile541Thr
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population: East Asian
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  num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
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X-46359403-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359403
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359403
    reference: chr 0
allele count: 2
allele frequency: 3.006524157421605e-5
allele num: 66522
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1621A>C
  hgvsp: ENSP00000429148.1:p.Ile541Leu
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1603A>C
  hgvsp: ENSP00000428248.1:p.Ile535Leu
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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population: Latino
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  allele num: 7425
  num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
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X-46359416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359416
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359416
    reference: chr 0
allele count: 1
allele frequency: 1.45985401459854e-5
allele num: 68500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1590G>A
  hgvsp: ENST00000414387.2:c.1590G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
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  hgvsp: ENST00000523374.1:c.1608G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  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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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val536Val
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 38052
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

X-46359427-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359427
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359427
    reference: chr 0
allele count: 1
allele frequency: 1.413747278536489e-5
allele num: 70734
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1597G>C
  hgvsp: ENSP00000429148.1:p.Ala533Pro
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1579G>C
  hgvsp: ENSP00000428248.1:p.Ala527Pro
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 239
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  variant carriers: 0
hgvs: p.Ala533Pro
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7348
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

X-46359432-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359432
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359432
    reference: chr 0
allele count: 1
allele frequency: 1.394000223040036e-5
allele num: 71736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1574G>T
  hgvsp: ENSP00000428248.1:p.Gly525Val
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1592G>T
  hgvsp: ENSP00000429148.1:p.Gly531Val
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  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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genotype quality: GenotypeQuality
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hgvs: p.Gly531Val
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3861
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

X-46359433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359433
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359433
    reference: chr 0
allele count: 1
allele frequency: 1.389525754859866e-5
allele num: 71967
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1573G>A
  hgvsp: ENSP00000428248.1:p.Gly525Arg
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1591G>A
  hgvsp: ENSP00000429148.1:p.Gly531Arg
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13914
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gly531Arg
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 511
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

X-46359443-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359443
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359443
    reference: chr 0
allele count: 1
allele frequency: 1.357810123832283e-5
allele num: 73648
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1581T>C
  hgvsp: ENST00000523374.1:c.1581T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1563T>C
  hgvsp: ENST00000414387.2:c.1563T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  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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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: 244
  bin: 8.25e1
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hgvs: p.Cys527Cys
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7428
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

X-46359462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359462
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359462
    reference: chr 0
allele count: 1
allele frequency: 1.307462998797134e-5
allele num: 76484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1544G>A
  hgvsp: ENSP00000428248.1:p.Gly515Glu
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1562G>A
  hgvsp: ENSP00000429148.1:p.Gly521Glu
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Gly521Glu
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8093
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

X-46359467-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359467
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359467
    reference: chr 0
allele count: 1
allele frequency: 1.291939588904823e-5
allele num: 77403
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1539T>G
  hgvsp: ENSP00000428248.1:p.His513Gln
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1557T>G
  hgvsp: ENSP00000429148.1:p.His519Gln
  variant of: http://identifiers.org/hgnc/17625
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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genotype quality: GenotypeQuality
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hgvs: p.His519Gln
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8819
  num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-46359484-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359484
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359484
    reference: chr 0
allele count: 1
allele frequency: 1.251705448673818e-5
allele num: 79891
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1540A>C
  hgvsp: ENSP00000429148.1:p.Lys514Gln
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1522A>C
  hgvsp: ENSP00000428248.1:p.Lys508Gln
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
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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: p.Lys514Gln
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8460
  num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

X-46359491-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359491
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359491
    reference: chr 0
allele count: 1
allele frequency: 1.236246754852269e-5
allele num: 80890
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1533T>G
  hgvsp: ENST00000523374.1:c.1533T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1515T>G
  hgvsp: ENST00000414387.2:c.1515T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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hgvs: p.Thr511Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4272
  num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

X-46359519-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359519
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359519
    reference: chr 0
allele count: 1
allele frequency: 1.19497155967688e-5
allele num: 83684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1487G>A
  hgvsp: ENSP00000428248.1:p.Cys496Tyr
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1505G>A
  hgvsp: ENSP00000429148.1:p.Cys502Tyr
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3350
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  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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  bin: 7.75e1
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 303
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys502Tyr
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8901
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

X-46359532-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359532
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359532
    reference: chr 0
allele count: 1
allele frequency: 1.182886005275672e-5
allele num: 84539
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1492G>T
  hgvsp: ENSP00000429148.1:p.Glu498Ter
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1474G>T
  hgvsp: ENSP00000428248.1:p.Glu492Ter
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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.Glu498Ter
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7860
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS

X-46359556-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359556
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359556
    reference: chr 0
allele count: 1
allele frequency: 1.167501430189252e-5
allele num: 85653
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1468A>G
  hgvsp: ENSP00000429148.1:p.Ile490Val
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1450A>G
  hgvsp: ENSP00000428248.1:p.Ile484Val
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.75e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Ile490Val
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.26151129052605e-4
  allele num: 7927
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

X-46359556-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359556
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359554
    reference: chr 0
allele count: 1
allele frequency: 1.167501430189252e-5
allele num: 85653
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1448_1449delGA
  hgvsp: ENSP00000428248.1:p.Arg483AsnfsTer9
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1466_1467delGA
  hgvsp: ENSP00000429148.1:p.Arg489AsnfsTer9
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 290
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  variant carriers: 0
hgvs: p.Arg489AsnfsTer9
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 611
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TTC
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-46359564-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359564
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359564
    reference: chr 0
allele count: 2
allele frequency: 2.327828020065877e-5
allele num: 85917
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1460A>G
  hgvsp: ENSP00000429148.1:p.His487Arg
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
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  hgvsp: ENSP00000428248.1:p.His481Arg
  variant of: http://identifiers.org/hgnc/17625
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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genotype quality: GenotypeQuality
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hgvs: p.His487Arg
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7937
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-46359588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359588
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359588
    reference: chr 0
allele count: 1
allele frequency: 1.157139551029854e-5
allele num: 86420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1418G>A
  hgvsp: ENSP00000428248.1:p.Ser473Asn
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1436G>A
  hgvsp: ENSP00000429148.1:p.Ser479Asn
  variant of: http://identifiers.org/hgnc/17625
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.Ser479Asn
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10038
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS

X-46359591-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359591
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359591
    reference: chr 0
allele count: 4
allele frequency: 4.62358258296441e-5
allele num: 86513
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1433T>C
  hgvsp: ENSP00000429148.1:p.Phe478Ser
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1415T>C
  hgvsp: ENSP00000428248.1:p.Phe472Ser
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: East Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 6544
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

X-46359607-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359607
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359607
    reference: chr 0
allele count: 2
allele frequency: 2.305050365350483e-5
allele num: 86766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1399G>C
  hgvsp: ENSP00000428248.1:p.Glu467Gln
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1417G>C
  hgvsp: ENSP00000429148.1:p.Glu473Gln
  variant of: http://identifiers.org/hgnc/17625
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.Glu473Gln
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7977
  num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-46359607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359607
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359607
    reference: chr 0
allele count: 6
allele frequency: 6.915151096051449e-5
allele num: 86766
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1417G>A
  hgvsp: ENSP00000429148.1:p.Glu473Lys
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1399G>A
  hgvsp: ENSP00000428248.1:p.Glu467Lys
  variant of: http://identifiers.org/hgnc/17625
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 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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  variant carriers: 4
hgvs: p.Glu473Lys
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 5
  allele frequency: 1.047208143090521e-4
  allele num: 47746
  num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

X-46359608-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359608
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359608
    reference: chr 0
allele count: 3
allele frequency: 3.456619426201175e-5
allele num: 86790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1398C>T
  hgvsp: ENST00000414387.2:c.1398C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1416C>T
  hgvsp: ENST00000523374.1:c.1416C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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.Asn472Asn
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7985
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

X-46359615-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359615
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359615
    reference: chr 0
allele count: 1
allele frequency: 1.150628818649392e-5
allele num: 86909
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1409A>T
  hgvsp: ENSP00000429148.1:p.Lys470Ile
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1391A>T
  hgvsp: ENSP00000428248.1:p.Lys464Ile
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Lys470Ile
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6589
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

X-46359640-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359640
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359638
    reference: chr 0
allele count: 1
allele frequency: 1.148791471372116e-5
allele num: 87048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1364_1365delGA
  hgvsp: ENSP00000428248.1:p.Arg455AsnfsTer9
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1382_1383delGA
  hgvsp: ENSP00000429148.1:p.Arg461AsnfsTer9
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
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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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hgvs: p.Arg461AsnfsTer9
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10092
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: TTC
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

X-46359650-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359650
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359650
    reference: chr 0
allele count: 1
allele frequency: 1.148659514346757e-5
allele num: 87058
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1374A>G
  hgvsp: ENST00000523374.1:c.1374A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1356A>G
  hgvsp: ENST00000414387.2:c.1356A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 105
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Val458Val
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6615
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

X-46359655-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359655
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359655
    reference: chr 0
allele count: 1
allele frequency: 1.148553970551076e-5
allele num: 87066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1351A>G
  hgvsp: ENSP00000428248.1:p.Ile451Val
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1369A>G
  hgvsp: ENSP00000429148.1:p.Ile457Val
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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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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hgvs: p.Ile457Val
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10095
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
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site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

X-46359673-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359673
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359673
    reference: chr 0
allele count: 9
allele frequency: 1.034066754753835e-4
allele num: 87035
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1333G>A
  hgvsp: ENSP00000428248.1:p.Gly445Arg
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1351G>A
  hgvsp: ENSP00000429148.1:p.Gly451Arg
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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hgvs: p.Gly451Arg
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6615
  num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
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site quality: MQ

X-46359700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359700
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359700
    reference: chr 0
allele count: 7
allele frequency: 8.037569898152507e-5
allele num: 87091
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1324G>T
  hgvsp: ENSP00000429148.1:p.Glu442Ter
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1306G>T
  hgvsp: ENSP00000428248.1:p.Glu436Ter
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
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  variant carriers: 0
genotype depth: GenotypeDepth
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hgvs: p.Glu442Ter
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 47948
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
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X-46359716-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359716
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359716
    reference: chr 0
allele count: 10
allele frequency: 1.148013362875544e-4
allele num: 87107
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1290A>G
  hgvsp: ENST00000414387.2:c.1290A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1308A>G
  hgvsp: ENST00000523374.1:c.1308A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 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: 155
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr436Thr
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47957
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

X-46359717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359717
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359717
    reference: chr 0
allele count: 1
allele frequency: 1.148039722174387e-5
allele num: 87105
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1307C>T
  hgvsp: ENSP00000429148.1:p.Thr436Ile
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1289C>T
  hgvsp: ENSP00000428248.1:p.Thr430Ile
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 311
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
hgvs: p.Thr436Ile
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47954
  num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

X-46359723-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359723
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359723
    reference: chr 0
allele count: 1
allele frequency: 1.148066082683719e-5
allele num: 87103
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1301C>G
  hgvsp: ENSP00000429148.1:p.Thr434Ser
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1283C>G
  hgvsp: ENSP00000428248.1:p.Thr428Ser
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Thr434Ser
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 627
  num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-46359728-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359728
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359728
    reference: chr 0
allele count: 2
allele frequency: 2.296000367360059e-5
allele num: 87108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1278T>C
  hgvsp: ENST00000414387.2:c.1278T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1296T>C
  hgvsp: ENST00000523374.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.His432His
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 2
  allele frequency: 1.978630787495053e-4
  allele num: 10108
  num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-46359729-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359729
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359729
    reference: chr 0
allele count: 119
allele frequency: 1.36597908559753e-3
allele num: 87117
alternate allele: C
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1295A>G
  hgvsp: ENSP00000429148.1:p.His432Arg
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1277A>G
  hgvsp: ENSP00000428248.1:p.His426Arg
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
hgvs: p.His432Arg
num of homozygotes: 1
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

X-46359734-GACAGAGAGGTGTGACTTTCCACTGAAAGTCTTCCCACATATACTACATTCATAGGGTTTCTCTCCTGTATGAATTCTCTGATGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359734
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359650
    reference: chr 0
allele count: 4
allele frequency: 4.592158888697549e-5
allele num: 87105
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsp: ENSP00000429148.1:p.Gln404_His431del
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsp: ENSP00000428248.1:p.Gln398_His425del
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln404_His431del
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4530
  num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: GACAGAGAGGTGTGACTTTCCACTGAAAGTCTTCCCACATATACTACATTCATAGGGTTTCTCTCCTGTATGAATTCTCTGATGA
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ

X-46359735-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359735
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359735
    reference: chr 0
allele count: 1
allele frequency: 1.148000183680029e-5
allele num: 87108
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1289T>C
  hgvsp: ENSP00000429148.1:p.Val430Ala
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1271T>C
  hgvsp: ENSP00000428248.1:p.Val424Ala
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51829
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val430Ala
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6622
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

X-46359754-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359754
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359754
    reference: chr 0
allele count: 1
allele frequency: 1.14796064790899e-5
allele num: 87111
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1270G>A
  hgvsp: ENSP00000429148.1:p.Gly424Arg
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1252G>A
  hgvsp: ENSP00000428248.1:p.Gly418Arg
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36930
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4304
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 30
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genotype quality: GenotypeQuality
  all individuals: 251
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 51872
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 24
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genotype quality: GenotypeQuality
  all individuals: 1784
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genotype quality: GenotypeQuality
  all individuals: 120
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genotype quality: GenotypeQuality
  all individuals: 157
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly424Arg
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.084810073802277e-5
  allele num: 47966
  num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

X-46359759-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359759
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359759
    reference: chr 0
allele count: 1
allele frequency: 1.147802532052386e-5
allele num: 87123
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1247T>G
  hgvsp: ENSP00000428248.1:p.Phe416Cys
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1265T>G
  hgvsp: ENSP00000429148.1:p.Phe422Cys
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
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genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
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genotype quality: GenotypeQuality
  all individuals: 4302
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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
  all individuals: 251
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51923
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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: 122
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genotype quality: GenotypeQuality
  all individuals: 26
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe422Cys
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47967
  num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

X-46359781-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359781
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359781
    reference: chr 0
allele count: 1
allele frequency: 1.147723490456679e-5
allele num: 87129
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1243T>A
  hgvsp: ENSP00000429148.1:p.Cys415Ser
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1225T>A
  hgvsp: ENSP00000428248.1:p.Cys409Ser
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 8.25e1
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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
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys415Ser
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.084592774801443e-5
  allele num: 47971
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-46359790-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359790
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359790
    reference: chr 0
allele count: 1
allele frequency: 1.147591778652498e-5
allele num: 87139
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1234C>T
  hgvsp: ENSP00000429148.1:p.Pro412Ser
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1216C>T
  hgvsp: ENSP00000428248.1:p.Pro406Ser
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
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  variant carriers: 0
hgvs: p.Pro412Ser
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 626
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-46359799-CTGTATGAATTCTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359799
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359785
    reference: chr 0
allele count: 1
allele frequency: 1.147749836445648e-5
allele num: 87127
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsp: ENSP00000428248.1:p.Gln398ArgfsTer6
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsp: ENSP00000429148.1:p.Gln404ArgfsTer6
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
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  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 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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genotype quality: GenotypeQuality
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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: 51929
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  variant carriers: 0
hgvs: p.Gln404ArgfsTer6
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7962
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: CTGTATGAATTCTCT
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

X-46359820-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359820
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359818
    reference: chr 0
allele count: 2
allele frequency: 2.295710464996155e-5
allele num: 87119
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1202_1203delCT
  hgvsp: ENSP00000429148.1:p.Ser401CysfsTer13
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1184_1185delCT
  hgvsp: ENSP00000428248.1:p.Ser395CysfsTer13
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
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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: 135
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genotype depth: GenotypeDepth
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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: 345
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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
  all individuals: 190
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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: 250
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
hgvs: p.Ser401CysfsTer13
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4530
  num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: CAG
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-46359821-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359821
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359821
    reference: chr 0
allele count: 1
allele frequency: 1.147842056932966e-5
allele num: 87120
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1203T>C
  hgvsp: ENST00000523374.1:c.1203T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1185T>C
  hgvsp: ENST00000414387.2:c.1185T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  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
  all individuals: 250
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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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  variant carriers: 0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Ser401Ser
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9308
  num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
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site quality: InbreedingCoeff

X-46359836-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359836
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359835
    reference: chr 0
allele count: 3
allele frequency: 3.444079627120979e-5
allele num: 87106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1169delG
  hgvsp: ENSP00000428248.1:p.Gly390GlufsTer89
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1187delG
  hgvsp: ENSP00000429148.1:p.Gly396GlufsTer89
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.25e1
  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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hgvs: p.Gly396GlufsTer89
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 3
  allele frequency: 6.254951836870857e-5
  allele num: 47962
  num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: TC
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
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site quality: MQ

X-46359846-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359846
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359846
    reference: chr 0
allele count: 115
allele frequency: 1.320776386815206e-3
allele num: 87070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1160G>A
  hgvsp: ENSP00000428248.1:p.Ser387Asn
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1178G>A
  hgvsp: ENSP00000429148.1:p.Ser393Asn
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Ser393Asn
num of homozygotes: 0
population: Other
  type: Population
  allele count: 6
  allele frequency: 9.584664536741214e-3
  allele num: 626
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
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X-46359873-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359873
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359873
    reference: chr 0
allele count: 2
allele frequency: 2.297952524300848e-5
allele num: 87034
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1151T>C
  hgvsp: ENSP00000429148.1:p.Ile384Thr
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1133T>C
  hgvsp: ENSP00000428248.1:p.Ile378Thr
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Ile384Thr
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9298
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
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X-46359876-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359876
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359876
    reference: chr 0
allele count: 1
allele frequency: 1.148791471372116e-5
allele num: 87048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1130A>G
  hgvsp: ENSP00000428248.1:p.Asn377Ser
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1148A>G
  hgvsp: ENSP00000429148.1:p.Asn383Ser
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50904
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4162
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn383Ser
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9298
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-46359880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359880
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359880
    reference: chr 0
allele count: 1
allele frequency: 1.148857461254782e-5
allele num: 87043
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1126G>A
  hgvsp: ENSP00000428248.1:p.Glu376Lys
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1144G>A
  hgvsp: ENSP00000429148.1:p.Glu382Lys
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
  all individuals: 36248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  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: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4160
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu382Lys
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6600
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

X-46359883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24046359883
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24046359883
    reference: chr 0
allele count: 1
allele frequency: 1.148870660141081e-5
allele num: 87042
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000429148
  ensembl transcript: ENST00000523374
  gene symbol: ZNF674
  hgvsc: ENST00000523374.1:c.1141A>G
  hgvsp: ENSP00000429148.1:p.Lys381Glu
  variant of: http://identifiers.org/hgnc/17625
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000251192
  ensembl protein: ENSP00000428248
  ensembl transcript: ENST00000414387
  gene symbol: ZNF674
  hgvsc: ENST00000414387.2:c.1123A>G
  hgvsp: ENSP00000428248.1:p.Lys375Glu
  variant of: http://identifiers.org/hgnc/17625
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
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genotype depth: GenotypeDepth
  all individuals: 64
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genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys381Glu
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 3301
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8491
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6013
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.3494032515741e-5
allele num: 42564
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.183e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

FS
type: SiteQuality
SIO_000300: 8.734e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

MQ
type: SiteQuality
SIO_000300: 5.216e1

DP
type: SiteQuality
SIO_000300: 1.471311e6

QD
type: SiteQuality
SIO_000300: 1.18e1

GenotypeQuality
all individuals: 1969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5664
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 12489
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3472
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.181977211479363e-4
allele num: 42302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5967
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7745
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.245e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.294e0

DP
type: SiteQuality
SIO_000300: 1.45409e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 7.109e0

MQRankSum
type: SiteQuality
SIO_000300: 6.54e-1

QD
type: SiteQuality
SIO_000300: 1.418e1

GenotypeQuality
all individuals: 386
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3942
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5953
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.118193000111819e-4
allele num: 8943
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7699
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.558e0

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.4437e6

QD
type: SiteQuality
SIO_000300: 2.806e1

MQ
type: SiteQuality
SIO_000300: 4.445e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeQuality
all individuals: 721
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1893
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variant carriers: 0

GenotypeQuality
all individuals: 5661
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7601
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8323
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4157
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 565
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.805382027871216e-5
allele num: 41620
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.819e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.793e1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.742e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
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SIO_000300: -6.02e-1

DP
type: SiteQuality
SIO_000300: 1.415725e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5889
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7602
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8323
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.127777151234916e-4
allele num: 8867
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.802727949475302e-5
allele num: 41643
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 565
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.410704e6

FS
type: SiteQuality
SIO_000300: 1.3715e1

MQ
type: SiteQuality
SIO_000300: 4.737e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.507e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.41e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1277
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.851660480799554e-5
allele num: 41223
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8772
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.193e0

VQSLOD
type: SiteQuality
SIO_000300: -1.489e0

DP
type: SiteQuality
SIO_000300: 1.379064e6

MQ
type: SiteQuality
SIO_000300: 4.822e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.819e1

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
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variant carriers: 0

GenotypeQuality
all individuals: 5665
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variant carriers: 3

GenotypeQuality
all individuals: 3139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.463296876539561e-5
allele num: 40596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8167
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 7.371007371007371e-4
allele num: 4070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5795
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.741e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

DP
type: SiteQuality
SIO_000300: 1.365203e6

FS
type: SiteQuality
SIO_000300: 1.015e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.713e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

MQ
type: SiteQuality
SIO_000300: 4.814e1

QD
type: SiteQuality
SIO_000300: 2.81e1

GenotypeQuality
all individuals: 3151
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5664
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5797
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.851488806245844e-5
allele num: 40603
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7485
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8165
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.137e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

DP
type: SiteQuality
SIO_000300: 1.365791e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.697e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2728
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.140786749482402e-3
allele num: 483
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 137
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4212
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.40184e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

MQ
type: SiteQuality
SIO_000300: 5.876e1

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.639e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.501e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.941e1

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 1.251788268955651e-2
allele num: 2796
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.462686567164179e-3
allele num: 134
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.370786516853932e-2
allele num: 89
num of homozygotes: 1

East Asian
type: Population
allele count: 2
allele frequency: 1.25e-2
allele num: 160
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.58288e5

MQ
type: SiteQuality
SIO_000300: 5.893e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.742e1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.669999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

Other
type: Population
allele count: 1
allele frequency: 1.123595505617977e-2
allele num: 89
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 481
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.73e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

QD
type: SiteQuality
SIO_000300: 2.805e1

DP
type: SiteQuality
SIO_000300: 1.56939e5

MQ
type: SiteQuality
SIO_000300: 5.866e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4445
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.518796992481203e-3
allele num: 133
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.42863e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.07e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.413e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1541
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1012
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 4.873294346978557e-4
allele num: 2052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1959
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13597
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.58e-2

QD
type: SiteQuality
SIO_000300: 6.36e0

MQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

MQ
type: SiteQuality
SIO_000300: 5.862e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-2

FS
type: SiteQuality
SIO_000300: 1.794e0

DP
type: SiteQuality
SIO_000300: 5.37917e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1641
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14065
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 199
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2149
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.065e1

DP
type: SiteQuality
SIO_000300: 5.73754e5

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.06e-2

QD
type: SiteQuality
SIO_000300: 1.425e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 199
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1075
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1655
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.039279177812192e-5
allele num: 14206
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.05e-2

DP
type: SiteQuality
SIO_000300: 5.82962e5

MQ
type: SiteQuality
SIO_000300: 5.715e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.343e0

VQSLOD
type: SiteQuality
SIO_000300: -9.899e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 2.235e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 229
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1335
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2161
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4485
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2227
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 6.63057e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.22e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.404e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2179
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16913
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.331378299120235e-4
allele num: 1364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 231
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.71781e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.25e-1

QD
type: SiteQuality
SIO_000300: 2.143e1

VQSLOD
type: SiteQuality
SIO_000300: -3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.23e-2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1513
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4809
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2273
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2726
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.06585e5

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.019e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21371
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3615
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5325
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.77294e5

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 1.611e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.52e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1985
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2621
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.323950361049855e-5
allele num: 23127
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 299
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3759
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.938e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.65e-1

DP
type: SiteQuality
SIO_000300: 8.12748e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.735e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

QD
type: SiteQuality
SIO_000300: 1.414e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2627
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1991
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 299
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.218e0

DP
type: SiteQuality
SIO_000300: 8.1772e5

QD
type: SiteQuality
SIO_000300: 2.07e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2309
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26531
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4259
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.35e0

VQSLOD
type: SiteQuality
SIO_000300: -1.651e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 5.569e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

DP
type: SiteQuality
SIO_000300: 8.82622e5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 353
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2617
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.405827153551471e-4
allele num: 28453
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
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allele num: 3030
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: -1.118e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 2.197e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

FS
type: SiteQuality
SIO_000300: 9.11e-1

DP
type: SiteQuality
SIO_000300: 9.1444e5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 397
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.984126984126984e-4
allele num: 5040
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6493
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3323
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6669
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MQRankSum
type: SiteQuality
SIO_000300: -5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

DP
type: SiteQuality
SIO_000300: 9.91048e5

VQSLOD
type: SiteQuality
SIO_000300: -2.131e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

QD
type: SiteQuality
SIO_000300: 2.095e1

Latino
type: Population
allele count: 1
allele frequency: 1.523461304082876e-4
allele num: 6564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5074
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3461
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3349
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.148e0

DP
type: SiteQuality
SIO_000300: 1.001153e6

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

FS
type: SiteQuality
SIO_000300: 7.025e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 409
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.01559060341968e-5
allele num: 33161
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5109
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3590
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6679
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

FS
type: SiteQuality
SIO_000300: 7.009e0

QD
type: SiteQuality
SIO_000300: 2.835e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.083e0

VQSLOD
type: SiteQuality
SIO_000300: -1.908e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.11e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.801e1

DP
type: SiteQuality
SIO_000300: 1.011368e6

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.977076510866329e-5
allele num: 33590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6771
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3715
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5164
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.431e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

DP
type: SiteQuality
SIO_000300: 1.020615e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

African
type: Population
allele count: 1
allele frequency: 1.427551748750892e-4
allele num: 7005
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5367
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4373
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35438
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

FS
type: SiteQuality
SIO_000300: 7.23e-1

QD
type: SiteQuality
SIO_000300: 2.046e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

DP
type: SiteQuality
SIO_000300: 1.067621e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

African
type: Population
allele count: 28
allele frequency: 3.984630710118116e-3
allele num: 7027
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.247191011235955e-3
allele num: 445
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35621
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5390
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4431
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3593
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.558e1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.88e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

DP
type: SiteQuality
SIO_000300: 1.075284e6

African
type: Population
allele count: 1
allele frequency: 1.40607424071991e-4
allele num: 7112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36435
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4747
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3645
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7312
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

FS
type: SiteQuality
SIO_000300: 1.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.0e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

DP
type: SiteQuality
SIO_000300: 1.094262e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3645
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7122
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36502
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Latino
type: Population
allele count: 1
allele frequency: 1.368176221097277e-4
allele num: 7309
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South Asian
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: 457
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.74e-1

FS
type: SiteQuality
SIO_000300: 7.025e0

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

DP
type: SiteQuality
SIO_000300: 1.098031e6

South Asian
type: Population
allele count: 1
allele frequency: 1.977066034005536e-4
allele num: 5058
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African
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allele count: 0
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Latino
type: Population
allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 471
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3685
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37002
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

DP
type: SiteQuality
SIO_000300: 1.106795e6

QD
type: SiteQuality
SIO_000300: 2.376e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7172
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5116
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.390254420008625e-5
allele num: 37104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3686
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5545
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VQSLOD
type: SiteQuality
SIO_000300: 3.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.109223e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

QD
type: SiteQuality
SIO_000300: 1.498e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

Latino
type: Population
allele count: 1
allele frequency: 1.317002502304754e-4
allele num: 7593
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3753
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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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: 486
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East Asian
type: Population
allele count: 0
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allele num: 5653
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.006e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

QD
type: SiteQuality
SIO_000300: 1.058e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

DP
type: SiteQuality
SIO_000300: 1.136102e6

FS
type: SiteQuality
SIO_000300: 5.783e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.05e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3823
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
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South Asian
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allele count: 1
allele frequency: 1.539408866995074e-4
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39084
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.551e1

DP
type: SiteQuality
SIO_000300: 1.163499e6

VQSLOD
type: SiteQuality
SIO_000300: -5.37e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.531325148715352e-5
allele num: 39505
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
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African
type: Population
allele count: 0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
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VQSLOD
type: SiteQuality
SIO_000300: -8.977000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.48e0

FS
type: SiteQuality
SIO_000300: 1.395e0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

DP
type: SiteQuality
SIO_000300: 1.177327e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6994
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5765
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.524296352391771e-5
allele num: 39615
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.342e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.456e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5829
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.551671344730799e-4
allele num: 3919
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40293
num of homozygotes: 0

South Asian
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: 525
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.18e1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -2.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.208257e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41717
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4039
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.325381047051027e-4
allele num: 7545
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FS
type: SiteQuality
SIO_000300: 5.195e0

DP
type: SiteQuality
SIO_000300: 1.262496e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.063e0

QD
type: SiteQuality
SIO_000300: 1.011e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.675322499581169e-4
allele num: 5969
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 553
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FS
type: SiteQuality
SIO_000300: 1.0209e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

QD
type: SiteQuality
SIO_000300: 1.423e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.927999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.280626e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7683
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6107
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9183
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.290845780262073e-5
allele num: 43652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.116e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.340631e6

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.233e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.259172239291524e-5
allele num: 44264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 585
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QD
type: SiteQuality
SIO_000300: 8.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

DP
type: SiteQuality
SIO_000300: 1.364542e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4413
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.576292559899117e-4
allele num: 6344
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7822
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45928
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.252e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.368e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.606e0

FS
type: SiteQuality
SIO_000300: 5.923e0

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

DP
type: SiteQuality
SIO_000300: 1.431419e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.98e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46431
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.562255897516013e-4
allele num: 6401
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9003
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4453
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MQ
type: SiteQuality
SIO_000300: 5.732e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

DP
type: SiteQuality
SIO_000300: 1.453413e6

QD
type: SiteQuality
SIO_000300: 2.848e1

FS
type: SiteQuality
SIO_000300: 0.0e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9135
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4495
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6481
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQ
type: SiteQuality
SIO_000300: 6.074e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

QD
type: SiteQuality
SIO_000300: 3.371e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

DP
type: SiteQuality
SIO_000300: 1.480297e6

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9135
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4495
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6481
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7927
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.007252215954875e-4
allele num: 9928
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47076
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.074e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

DP
type: SiteQuality
SIO_000300: 1.480297e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

QD
type: SiteQuality
SIO_000300: 3.371e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

South Asian
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allele count: 0
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allele num: 9969
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
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Latino
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allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.235672836630099e-5
allele num: 47218
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East Asian
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.022e0

DP
type: SiteQuality
SIO_000300: 1.488385e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.6e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 3.226e0

VQSLOD
type: SiteQuality
SIO_000300: -2.401e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

QD
type: SiteQuality
SIO_000300: 2.705e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9218
num of homozygotes: 0

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: 617
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East Asian
type: Population
allele count: 1
allele frequency: 1.531393568147014e-4
allele num: 6530
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.215e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 0.0e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
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European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.406010297362615e-5
allele num: 47585
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
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South Asian
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.443e1

Other
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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
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Latino
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South Asian
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allele count: 2
allele frequency: 1.986689182477401e-4
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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QD
type: SiteQuality
SIO_000300: 1.64e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.642e-1

East Asian
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allele num: 6573
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Latino
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allele frequency: 1.08038029386344e-4
allele num: 9256
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African
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4524
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South Asian
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allele count: 0
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Other
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.787e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.642e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

DP
type: SiteQuality
SIO_000300: 1.523795e6

East Asian
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allele count: 1
allele frequency: 1.521606816798539e-4
allele num: 6572
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
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allele num: 623
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.186991018904265e-5
allele num: 47767
num of homozygotes: 0

Latino
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South Asian
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DP
type: SiteQuality
SIO_000300: 1.525074e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.584e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.71e-1

QD
type: SiteQuality
SIO_000300: 1.774e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.86e-2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

South Asian
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Latino
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Other
type: Population
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African
type: Population
allele count: 1
allele frequency: 1.251251251251251e-4
allele num: 7992
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47837
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

FS
type: SiteQuality
SIO_000300: 2.921e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 3.082e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.14e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Latino
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African
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allele count: 0
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European (Non-Finnish)
type: Population
allele count: 0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.511715797430083e-4
allele num: 6615
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Other
type: Population
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allele num: 627
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.426e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

MQ
type: SiteQuality
SIO_000300: 6.046e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7983
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086637175527919e-5
allele num: 47924
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Other
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Latino
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South Asian
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.025e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 3.099e1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.534456e6

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: 4528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
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: 47931
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.252975817566721e-4
allele num: 7981
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 1.854e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.41e-1

DP
type: SiteQuality
SIO_000300: 1.535365e6

FS
type: SiteQuality
SIO_000300: 4.335e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

African
type: Population
allele count: 8
allele frequency: 1.004394224733208e-3
allele num: 7965
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10089
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.07654214662504e-4
allele num: 9289
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47923
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.538281e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.481e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.36e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.527e1

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 8.780732563973909e-4
allele num: 7972
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

QD
type: SiteQuality
SIO_000300: 1.58e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.34e-2

DP
type: SiteQuality
SIO_000300: 1.541591e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

FS
type: SiteQuality
SIO_000300: 1.101e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.32e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10105
num of homozygotes: 0

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: 4530
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.128526645768025e-3
allele num: 7975
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.075962986873252e-4
allele num: 9294
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

FS
type: SiteQuality
SIO_000300: 2.446e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 1.542315e6

QD
type: SiteQuality
SIO_000300: 1.596e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.451e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.253918495297806e-4
allele num: 7975
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10105
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

QD
type: SiteQuality
SIO_000300: 2.674e1

MQ
type: SiteQuality
SIO_000300: 5.851e1

VQSLOD
type: SiteQuality
SIO_000300: -2.443e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.483e0

DP
type: SiteQuality
SIO_000300: 1.541736e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10105
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47956
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.511258878645912e-4
allele num: 6617
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.54213e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.116e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.801e0

FS
type: SiteQuality
SIO_000300: 5.213e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.32e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

QD
type: SiteQuality
SIO_000300: 8.050000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7969
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47959
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 5.182e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

DP
type: SiteQuality
SIO_000300: 1.542095e6

QD
type: SiteQuality
SIO_000300: 3.28e0

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

African
type: Population
allele count: 116
allele frequency: 1.455275373227951e-2
allele num: 7971
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10109
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.151000215100022e-4
allele num: 9298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085070892410342e-5
allele num: 47960
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.275e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

QD
type: SiteQuality
SIO_000300: 1.746e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 1.550931e6

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

Latino
type: Population
allele count: 4
allele frequency: 4.302000430200043e-4
allele num: 9298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47957
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7967
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10107
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

DP
type: SiteQuality
SIO_000300: 1.547822e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: -2.283e0

FS
type: SiteQuality
SIO_000300: 7.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.185e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.79e-2

QD
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQ
type: SiteQuality
SIO_000300: 5.835e1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084983945623619e-5
allele num: 47962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7967
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9293
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10107
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 6.26e0

DP
type: SiteQuality
SIO_000300: 1.547386e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9293
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.547948e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.268e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7967
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.886307464162135e-5
allele num: 10115
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 4.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

QD
type: SiteQuality
SIO_000300: 3.464e1

DP
type: SiteQuality
SIO_000300: 1.548145e6

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 5.52e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.548548e6

FS
type: SiteQuality
SIO_000300: 3.247e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9307
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084549320436922e-5
allele num: 47972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.729000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.548576e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.938e0

QD
type: SiteQuality
SIO_000300: 2.934e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47971
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.881422924901186e-5
allele num: 10120
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9301
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6617
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 4.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

MQ
type: SiteQuality
SIO_000300: 4.582e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.548155e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.976479889317126e-4
allele num: 10119
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6611
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47967
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.203e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.065e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -4.209e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQ
type: SiteQuality
SIO_000300: 6.112e1

QD
type: SiteQuality
SIO_000300: 3.004e1

DP
type: SiteQuality
SIO_000300: 1.548046e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

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: 10115
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7959
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47968
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.597444089456869e-3
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.132e0

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.058e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 1.547842e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6609
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10119
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.546388e6

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

QD
type: SiteQuality
SIO_000300: 3.314e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.94e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQ
type: SiteQuality
SIO_000300: 6.04e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 5.214851898206091e-4
allele num: 47940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7955
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 84
allele frequency: 1.855123674911661e-2
allele num: 4528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.553109e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.445e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.663e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.034e1

QD
type: SiteQuality
SIO_000300: 1.926e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10113
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.032600454890068e-4
allele num: 6595
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: 7942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.82e-2

QD
type: SiteQuality
SIO_000300: 1.621e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.572e0

MQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 1.5422e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6603
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7943
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.889240506329114e-5
allele num: 10112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.654e-1

QD
type: SiteQuality
SIO_000300: 3.439e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.541793e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075615790039798e-4
allele num: 9297
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47939
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10113
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.269e0

QD
type: SiteQuality
SIO_000300: 6.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.542205e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 6.385e0