X-47028928-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047028928
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047028928
    reference: chr 0
allele count: 1
allele frequency: 2.808830964552553e-5
allele num: 35602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+31G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+31G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.201+31G>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

X-47030380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030380
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030380
    reference: chr 0
allele count: 1
allele frequency: 1.393961359391118e-5
allele num: 71738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1483C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.202-47C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1483C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

X-47030394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030394
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030394
    reference: chr 0
allele count: 1
allele frequency: 1.382150903235615e-5
allele num: 72351
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.202-33G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1497G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1497G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11479
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-47030435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030435
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030435
    reference: chr 0
allele count: 2
allele frequency: 2.64120544616563e-5
allele num: 75723
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1538C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.210C>T
  hgvsp: ENST00000377604.3:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1538C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5151
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Tyr70Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

X-47030441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030441
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030441
    reference: chr 0
allele count: 1
allele frequency: 1.313956849657057e-5
allele num: 76106
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.216C>T
  hgvsp: ENST00000377604.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1544C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1544C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 195
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genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 564
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genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala72Ala
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

X-47030442-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030442
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030442
    reference: chr 0
allele count: 1
allele frequency: 1.313853268866933e-5
allele num: 76112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1545T>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1545T>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.217T>G
  hgvsp: ENSP00000366829.3:p.Ser73Ala
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser73Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

X-47030446-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030446
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030446
    reference: chr 0
allele count: 2
allele frequency: 2.620407735443635e-5
allele num: 76324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.221C>T
  hgvsp: ENSP00000366829.3:p.Pro74Leu
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1549C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1549C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1816
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro74Leu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

X-47030447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030447
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030447
    reference: chr 0
allele count: 1
allele frequency: 1.307343347583376e-5
allele num: 76491
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1550G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.222G>A
  hgvsp: ENST00000377604.3:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1550G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
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  variant carriers: 1
hgvs: p.Pro74Pro
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

X-47030453-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030453
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030453
    reference: chr 0
allele count: 7
allele frequency: 9.114227308829082e-5
allele num: 76803
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1556C>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.228C>G
  hgvsp: ENST00000377604.3:c.228C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1556C>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser76Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

X-47030453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030453
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030453
    reference: chr 0
allele count: 1
allele frequency: 1.302032472689869e-5
allele num: 76803
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1556C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.228C>T
  hgvsp: ENST00000377604.3:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1556C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Ser76Ser
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-47030463-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030463
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030463
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 76762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1566C>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.238C>A
  hgvsp: ENSP00000366829.3:p.Arg80Ser
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1566C>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg80Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

X-47030466-AGGC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030466
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030463
    reference: chr 0
allele count: 21
allele frequency: 2.767418262324895e-4
allele num: 75883
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.254_256delGGC
  hgvsp: ENSP00000366829.3:p.Arg85del
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1582_201+1584delGGC
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1582_201+1584delGGC
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6675
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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
  all individuals: 251
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hgvs: p.Arg85del
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: AGGC
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

X-47030472-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030472
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030472
    reference: chr 0
allele count: 4
allele frequency: 5.248655032148012e-5
allele num: 76210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1575C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.247C>T
  hgvsp: ENSP00000366829.3:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1575C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Arg83Trp
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

X-47030475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030475
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030475
    reference: chr 0
allele count: 1
allele frequency: 1.309328968903437e-5
allele num: 76375
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1578C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1578C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.250C>T
  hgvsp: ENSP00000366829.3:p.Arg84Trp
  variant of: http://identifiers.org/hgnc/9896
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 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: 542
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  variant carriers: 0
hgvs: p.Arg84Trp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-47030476-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030476
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030476
    reference: chr 0
allele count: 2
allele frequency: 2.618452232885142e-5
allele num: 76381
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1579G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1579G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.251G>A
  hgvsp: ENSP00000366829.3:p.Arg84Gln
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Arg84Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-47030477-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030477
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030477
    reference: chr 0
allele count: 2
allele frequency: 2.613183510812047e-5
allele num: 76535
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1580G>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.252G>C
  hgvsp: ENST00000377604.3:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1580G>C
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1641
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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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  variant carriers: 0
hgvs: p.Arg84Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

X-47030478-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030478
    reference: chr 0
allele count: 2
allele frequency: 2.616294280780702e-5
allele num: 76444
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.253C>A
  hgvsp: ENST00000377604.3:c.253C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1581C>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1581C>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 212
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg85Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

X-47030478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030478
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 76444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1581C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.253C>T
  hgvsp: ENSP00000366829.3:p.Arg85Trp
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1581C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg85Trp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
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X-47030486-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030486
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030486
    reference: chr 0
allele count: 1
allele frequency: 1.306182160164057e-5
allele num: 76559
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1589G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.261G>A
  hgvsp: ENST00000377604.3:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1589G>A
  variant of: http://identifiers.org/hgnc/9896
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 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.Arg87Arg
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

X-47030495-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030495
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030495
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 76431
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1598C>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1598C>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.270C>A
  hgvsp: ENST00000377604.3:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Pro90Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

X-47030498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030498
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030498
    reference: chr 0
allele count: 1
allele frequency: 1.307377531409745e-5
allele num: 76489
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1601C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1601C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.273C>T
  hgvsp: ENST00000377604.3:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 542
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr91Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

X-47030499-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030499
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030499
    reference: chr 0
allele count: 4
allele frequency: 5.232109455729814e-5
allele num: 76451
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1602G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1602G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.274G>A
  hgvsp: ENSP00000366829.3:p.Gly92Ser
  variant of: http://identifiers.org/hgnc/9896
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Gly92Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

X-47030504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030504
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030504
    reference: chr 0
allele count: 1
allele frequency: 1.304954913807728e-5
allele num: 76631
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.279G>A
  hgvsp: ENST00000377604.3:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1607G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1607G>A
  variant of: http://identifiers.org/hgnc/9896
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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hgvs: p.Pro93Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-47030504-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030504
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030504
    reference: chr 0
allele count: 1
allele frequency: 1.304954913807728e-5
allele num: 76631
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1607G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1607G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.279G>T
  hgvsp: ENST00000377604.3:c.279G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Pro93Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
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site quality: MQ

X-47030516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030516
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030516
    reference: chr 0
allele count: 2
allele frequency: 2.594403870850575e-5
allele num: 77089
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1619C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.291C>T
  hgvsp: ENST00000377604.3:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1619C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro97Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

X-47030522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030522
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030522
    reference: chr 0
allele count: 1
allele frequency: 1.294314078254229e-5
allele num: 77261
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1625C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.297C>T
  hgvsp: ENST00000377604.3:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1625C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 90
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
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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
  all individuals: 2032
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 13029
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3405
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 2409
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1914
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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: 930
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp99Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

X-47030533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030533
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030533
    reference: chr 0
allele count: 3
allele frequency: 3.870218667354705e-5
allele num: 77515
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.308G>A
  hgvsp: ENSP00000366829.3:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1636G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1636G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 264
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
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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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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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
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
  all individuals: 1899
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg103Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

X-47030534-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030534
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030534
    reference: chr 0
allele count: 1
allele frequency: 1.28783000643915e-5
allele num: 77650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1637G>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.309G>C
  hgvsp: ENST00000377604.3:c.309G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1637G>C
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 177
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5597
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg103Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

X-47030540-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030540
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030540
    reference: chr 0
allele count: 6
allele frequency: 7.730265276936753e-5
allele num: 77617
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.315G>A
  hgvsp: ENST00000377604.3:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1643G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1643G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 3.25e1
  variant carriers: 2
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 quality: GenotypeQuality
  all individuals: 1868
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 550
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln105Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

X-47030553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030553
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030553
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 76882
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.328G>A
  hgvsp: ENSP00000366829.3:p.Glu110Lys
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1656G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1656G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11390
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16994
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14664
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3618
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu110Lys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

X-47030560-GGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030560
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030557
    reference: chr 0
allele count: 1635
allele frequency: 2.484236116386842e-2
allele num: 65815
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1685_201+1687delGGA
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1685_201+1687delGGA
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.357_359delGGA
  hgvsp: ENSP00000366829.3:p.Glu119del
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 1.25e1
  variant carriers: 503
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 3.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.25e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 1.75e1
  variant carriers: 735
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 7.5e0
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 2.25e1
  variant carriers: 553
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 2.75e1
  variant carriers: 375
genotype quality: GenotypeQuality
  all individuals: 3476
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 3.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 10730
  bin: 6.25e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 4.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 2.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3941
  bin: 3.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 6225
  bin: 2.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 13769
  bin: 2.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 6.75e1
  variant carriers: 94
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.25e1
  variant carriers: 181
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 1.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 4.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 7.25e1
  variant carriers: 141
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 8.75e1
  variant carriers: 201
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 7.75e1
  variant carriers: 160
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 195
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 51
hgvs: p.Glu119del
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: GGGA
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-47030560-G-GGGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030560
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030563
    reference: chr 0
allele count: 5
allele frequency: 7.597052343690648e-5
allele num: 65815
alternate allele: GGGA
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.357_359dupGGA
  hgvsp: ENSP00000366829.3:p.Glu119dup
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1685_201+1687dupGGA
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1685_201+1687dupGGA
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13769
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6225
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3476
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3941
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2415
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu119dup
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

X-47030560-GGGAGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030560
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030554
    reference: chr 0
allele count: 2
allele frequency: 3.038820937476259e-5
allele num: 65815
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.354_359delGGAGGA
  hgvsp: ENSP00000366829.3:p.Glu118_Glu119del
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3476
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3941
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6225
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13769
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2415
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu118_Glu119del
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: GGGAGGA
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

X-47030573-G-GGAGGAGGAGGAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030573
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030585
    reference: chr 0
allele count: 1
allele frequency: 1.332853506071148e-5
allele num: 75027
alternate allele: GGAGGAGGAGGAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsp: ENSP00000366829.3:p.Asp120_Glu123dup
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 10945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
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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  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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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4797
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp120_Glu123dup
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

X-47030576-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030576
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030576
    reference: chr 0
allele count: 1
allele frequency: 1.333031179599291e-5
allele num: 75017
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1679G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.351G>T
  hgvsp: ENSP00000366829.3:p.Glu117Asp
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1679G>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
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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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  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
  all individuals: 13
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2527
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genotype quality: GenotypeQuality
  all individuals: 4800
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 307
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu117Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

X-47030579-GGAGGAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030579
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030573
    reference: chr 0
allele count: 1
allele frequency: 1.357220412595005e-5
allele num: 73680
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.360_365delTGAGGA
  hgvsp: ENSP00000366829.3:p.Asp120_Glu121del
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9170
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1383
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 350
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
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  variant carriers: 0
hgvs: p.Asp120_Glu121del
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: GGAGGAT
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

X-47030582-GGAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030582
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030579
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 68285
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.360_362delTGA
  hgvsp: ENSP00000366829.3:p.Asp120del
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1688_201+1690delTGA
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1688_201+1690delTGA
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe deletion
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 9010
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 117
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 212
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genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 506
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  all individuals: 1015
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2486
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp120del
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: GGAT
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

X-47030583-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030583
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030583
    reference: chr 0
allele count: 1
allele frequency: 1.349964900912576e-5
allele num: 74076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1686G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.358G>A
  hgvsp: ENSP00000366829.3:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1686G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp120Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

X-47030585-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030585
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030585
    reference: chr 0
allele count: 10
allele frequency: 1.627630658051075e-4
allele num: 61439
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1688T>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.360T>G
  hgvsp: ENSP00000366829.3:p.Asp120Glu
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1688T>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 183
  bin: 9.25e1
  variant carriers: 2
hgvs: p.Asp120Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

X-47030585-T-TGAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030585
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030588
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 61439
alternate allele: TGAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1701_201+1703dupGAG
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1701_201+1703dupGAG
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.373_375dupGAG
  hgvsp: ENSP00000366829.3:p.Glu125dup
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe insertion
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu125dup
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-47030585-TGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030585
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030582
    reference: chr 0
allele count: 154
allele frequency: 2.506551213398656e-3
allele num: 61439
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1701_201+1703delGAG
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.373_375delGAG
  hgvsp: ENSP00000366829.3:p.Glu125del
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1701_201+1703delGAG
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9019
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  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 3.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 373
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genotype depth: GenotypeDepth
  all individuals: 237
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  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2058
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 503
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genotype quality: GenotypeQuality
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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: 3615
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 4013
  bin: 2.75e1
  variant carriers: 12
hgvs: p.Glu125del
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: TGAG
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

X-47030619-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030619
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030619
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 72429
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1722A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.394A>G
  hgvsp: ENSP00000366829.3:p.Met132Val
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1722A>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met132Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
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site quality: BaseQRankSum
site quality: ReadPosRankSum
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X-47030658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030658
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030658
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 72496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1761G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.432+1G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
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  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1761G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: splice donor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.432+1G>A
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
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site quality: ClippingRankSum
site quality: FS
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X-47030678-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030678
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030678
    reference: chr 0
allele count: 30
allele frequency: 4.26081892939823e-4
allele num: 70409
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1781C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1781C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000182872
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
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site quality: DP
site quality: MQRankSum
site quality: VQSLOD
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site quality: ClippingRankSum
site quality: FS
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site quality: QD

X-47030679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030679
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030679
    reference: chr 0
allele count: 1
allele frequency: 1.422616761270681e-5
allele num: 70293
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.432+22G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1782G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
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  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1782G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
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population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
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site quality: ClippingRankSum
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X-47030685-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030685
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030685
    reference: chr 0
allele count: 1
allele frequency: 1.430144587617808e-5
allele num: 69923
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1788G>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.432+28G>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1788G>C
  variant of: http://identifiers.org/hgnc/9896
canonical: true
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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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  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

X-47030706-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030706
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030706
    reference: chr 0
allele count: 1
allele frequency: 1.508773518007212e-5
allele num: 66279
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.432+49C>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1809C>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1809C>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
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site quality: BaseQRankSum

X-47030709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047030709
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047030709
    reference: chr 0
allele count: 1
allele frequency: 1.5148760831364e-5
allele num: 66012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.201+1812G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.432+52G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
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  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.201+1812G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-47032476-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032476
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032476
    reference: chr 0
allele count: 4
allele frequency: 4.884541646823216e-5
allele num: 81891
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-51C>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-51C>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-51C>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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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num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

X-47032481-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032481
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032481
    reference: chr 0
allele count: 3
allele frequency: 3.657599882956804e-5
allele num: 82021
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-46G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-46G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-46G>A
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
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site quality: FS
site quality: DP
site quality: ReadPosRankSum

X-47032481-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032481
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032481
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 82021
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-46G>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-46G>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-46G>C
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
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X-47032499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032499
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032499
    reference: chr 0
allele count: 1
allele frequency: 1.20296410355115e-5
allele num: 83128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-28C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-28C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
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  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-28C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
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site quality: FS
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X-47032500-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032500
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032500
    reference: chr 0
allele count: 2
allele frequency: 2.402950823611395e-5
allele num: 83231
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-27T>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-27T>C
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-27T>C
  variant of: http://identifiers.org/hgnc/9896
canonical: true
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
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X-47032504-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032504
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032504
    reference: chr 0
allele count: 1
allele frequency: 1.194386383995222e-5
allele num: 83725
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-23C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-23C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: Other
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population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
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X-47032520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032520
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032520
    reference: chr 0
allele count: 1
allele frequency: 1.175184797809456e-5
allele num: 85093
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-7C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-7C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-7C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
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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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  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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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 7.25e1
  variant carriers: 0
hgvs: c.433-7C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

X-47032523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032523
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032523
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 85378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.202-4A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.433-4A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.202-4A>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
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  variant carriers: 0
hgvs: c.433-4A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

X-47032546-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032546
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032546
    reference: chr 0
allele count: 1
allele frequency: 1.160025520561452e-5
allele num: 86205
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.221C>T
  hgvsp: ENSP00000328848.7:p.Ser74Leu
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.452C>T
  hgvsp: ENSP00000366829.3:p.Ser151Leu
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.221C>T
  hgvsp: ENSP00000329659.6:p.Ser74Leu
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
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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 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.Ser151Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

X-47032550-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032550
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032550
    reference: chr 0
allele count: 1
allele frequency: 1.159958241503306e-5
allele num: 86210
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.456C>T
  hgvsp: ENST00000377604.3:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.225C>T
  hgvsp: ENST00000329236.7:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.225C>T
  hgvsp: ENST00000345781.6:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype 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: 8230
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  variant carriers: 1
hgvs: p.His152His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

X-47032563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032563
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032563
    reference: chr 0
allele count: 1
allele frequency: 1.164307004470939e-5
allele num: 85888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.238C>T
  hgvsp: ENSP00000329659.6:p.Arg80Trp
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.469C>T
  hgvsp: ENSP00000366829.3:p.Arg157Trp
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.238C>T
  hgvsp: ENSP00000328848.7:p.Arg80Trp
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 8.25e1
  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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg157Trp
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

X-47032589-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032589
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032589
    reference: chr 0
allele count: 3
allele frequency: 3.587443946188341e-5
allele num: 83625
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.264A>G
  hgvsp: ENST00000345781.6:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.264A>G
  hgvsp: ENST00000329236.7:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.495A>G
  hgvsp: ENST00000377604.3:c.495A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 339
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  variant carriers: 0
hgvs: p.Lys165Lys
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

X-47032591-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032591
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032591
    reference: chr 0
allele count: 1
allele frequency: 1.201230059581011e-5
allele num: 83248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.266C>T
  hgvsp: ENSP00000329659.6:p.Ser89Phe
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.497C>T
  hgvsp: ENSP00000366829.3:p.Ser166Phe
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.266C>T
  hgvsp: ENSP00000328848.7:p.Ser89Phe
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 3.25e1
  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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
hgvs: p.Ser166Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

X-47032600-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032600
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032600
    reference: chr 0
allele count: 1
allele frequency: 1.230996491659999e-5
allele num: 81235
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+4A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.502+4A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.271+4A>G
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 1075
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  variant carriers: 0
hgvs: c.502+4A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

X-47032613-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032613
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032613
    reference: chr 0
allele count: 5
allele frequency: 6.424670735624799e-5
allele num: 77825
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.502+17G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.271+17G>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+17G>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10642
  bin: 2.75e1
  variant carriers: 0
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
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X-47032621-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032621
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032621
    reference: chr 0
allele count: 1
allele frequency: 1.339369424874769e-5
allele num: 74662
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+25C>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000182872
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
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X-47032622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032622
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032622
    reference: chr 0
allele count: 2
allele frequency: 2.698472664471909e-5
allele num: 74116
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.502+26C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+26C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  ensembl gene: ENSG00000182872
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: FS
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X-47032631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032631
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032631
    reference: chr 0
allele count: 1
allele frequency: 1.454101292696049e-5
allele num: 68771
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.502+35G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+35G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
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X-47032638-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032638
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032638
    reference: chr 0
allele count: 1
allele frequency: 1.64446637066272e-5
allele num: 60810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+42C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.271+42C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.502+42C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
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X-47032648-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032648
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047032648
    reference: chr 0
allele count: 1
allele frequency: 1.888146218043125e-5
allele num: 52962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.271+52G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
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  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.271+52G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  ensembl gene: ENSG00000182872
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
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X-47032648-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047032648
    reference: chr 0
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    type: ExactPosition
    position: 24047032648
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 52962
alternate allele: C
annotation: Annotation
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  ensembl protein: ENSP00000366829
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  ensembl gene: ENSG00000182872
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  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/9896
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num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
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site quality: InbreedingCoeff
site quality: MQRankSum
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X-47034370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034370
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047034370
    reference: chr 0
allele count: 1
allele frequency: 1.148936659121983e-5
allele num: 87037
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.272-48A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.503-48A>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
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  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
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population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
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site quality: DP
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X-47034371-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034371
    reference: chr 0
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    type: ExactPosition
    position: 24047034371
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allele count: 2
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allele num: 87049
alternate allele: G
annotation: Annotation
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  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
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  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/9896
canonical: true
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

X-47034392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034392
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047034392
    reference: chr 0
allele count: 1
allele frequency: 1.147065233599835e-5
allele num: 87179
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.503-26C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.272-26C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.272-26C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

X-47034443-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034443
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047034443
    reference: chr 0
allele count: 1
allele frequency: 1.141800162135623e-5
allele num: 87581
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182872
  ensembl transcript: ENST00000496012
  gene symbol: RBM10
  hgvsc: ENST00000496012.2:n.33C>G
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.528C>G
  hgvsp: ENST00000377604.3:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.297C>G
  hgvsp: ENST00000329236.7:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.297C>G
  hgvsp: ENST00000345781.6:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Val176Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

X-47034446-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034446
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047034446
    reference: chr 0
allele count: 2
allele frequency: 2.283391750105607e-5
allele num: 87589
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.531G>A
  hgvsp: ENST00000377604.3:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182872
  ensembl transcript: ENST00000496012
  gene symbol: RBM10
  hgvsc: ENST00000496012.2:n.36G>A
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.300G>A
  hgvsp: ENST00000345781.6:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.300G>A
  hgvsp: ENST00000329236.7:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 497
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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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hgvs: p.Glu177Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
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X-47034502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034502
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047034502
    reference: chr 0
allele count: 7
allele frequency: 8.019981210329735e-5
allele num: 87282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl transcript: ENST00000496012
  gene symbol: RBM10
  hgvsc: ENST00000496012.2:n.81+11C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.345+11C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.576+11C>T
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.345+11C>T
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-47034511-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047034511
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047034512
    reference: chr 0
allele count: 378
allele frequency: 4.446012702893437e-3
allele num: 85020
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000329659
  ensembl transcript: ENST00000345781
  gene symbol: RBM10
  hgvsc: ENST00000345781.6:c.345+29dupC
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000366829
  ensembl transcript: ENST00000377604
  gene symbol: RBM10
  hgvsc: ENST00000377604.3:c.576+29dupC
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl transcript: ENST00000496012
  gene symbol: RBM10
  hgvsc: ENST00000496012.2:n.81+29dupC
  variant of: http://identifiers.org/hgnc/9896
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182872
  ensembl protein: ENSP00000328848
  ensembl transcript: ENST00000329236
  gene symbol: RBM10
  hgvsc: ENST00000329236.7:c.345+29dupC
  variant of: http://identifiers.org/hgnc/9896
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 4.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 5.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 3.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 9730
  bin: 3.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 1.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 8.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 4.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 3.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 9.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 2.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 13058
  bin: 9.75e1
  variant carriers: 198
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 1.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 1.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.5e0
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 5362
  bin: 6.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 7.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 7.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 18768
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 5.75e1
  variant carriers: 22
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.249619402593312e-5
allele num: 19049
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2681
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2405
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1009
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4457
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 279
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

FS
type: SiteQuality
SIO_000300: 4.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.77767e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.61e-2

QD
type: SiteQuality
SIO_000300: 4.63e0

VQSLOD
type: SiteQuality
SIO_000300: -1.619e0

GenotypeQuality
all individuals: 9303
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5905
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.18427285646613e-4
allele num: 8444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39117
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e0

DP
type: SiteQuality
SIO_000300: 1.142368e6

VQSLOD
type: SiteQuality
SIO_000300: 1.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

FS
type: SiteQuality
SIO_000300: 3.214e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.093e1

GenotypeQuality
all individuals: 1756
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6197
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5957
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.533377245205584e-5
allele num: 39473
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8459
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8595
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.566e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.192988e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.51e-1

GenotypeQuality
all individuals: 1958
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.837227301310889e-5
allele num: 41346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8945
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.827e1

DP
type: SiteQuality
SIO_000300: 1.326007e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

GenotypeQuality
all individuals: 1289
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 517
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6211
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.407202349429493e-5
allele num: 41542
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.724e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 1.177e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.19e-1

DP
type: SiteQuality
SIO_000300: 1.331287e6

VQSLOD
type: SiteQuality
SIO_000300: -2.963e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.798e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 1.041e1

GenotypeQuality
all individuals: 1672
bin: 3.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.40633346969223e-5
allele num: 41557
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 517
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8759
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9011
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.729e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 1.334082e6

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

QD
type: SiteQuality
SIO_000300: 1.04e1

FS
type: SiteQuality
SIO_000300: 4.795e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.79e-1

GenotypeQuality
all individuals: 871
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9043
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41636
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.139081899988609e-4
allele num: 8779
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6658
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.605136436597111e-4
allele num: 6230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3457
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 9.11e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

DP
type: SiteQuality
SIO_000300: 1.342341e6

GenotypeQuality
all individuals: 707
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 525
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6243
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.137527016266636e-4
allele num: 8791
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41727
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9057
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 8.289999999999999e0

FS
type: SiteQuality
SIO_000300: 1.0108e1

VQSLOD
type: SiteQuality
SIO_000300: -1.563e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

DP
type: SiteQuality
SIO_000300: 1.344516e6

GenotypeQuality
all individuals: 909
bin: 3.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6271
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.670524783428394e-4
allele num: 41903
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9085
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6729
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3475
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

FS
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.348209e6

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.486104919007282e-4
allele num: 6729
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3475
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6271
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41903
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9085
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

QD
type: SiteQuality
SIO_000300: 1.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.348209e6

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6745
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41833
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.340492e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: -3.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.737e0

QD
type: SiteQuality
SIO_000300: 2.574e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 5

South Asian
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allele count: 3
allele frequency: 3.325942350332594e-4
allele num: 9020
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3412
num of homozygotes: 0

Latino
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allele count: 5
allele frequency: 5.74052812858783e-4
allele num: 8710
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.933254392112322e-4
allele num: 41381
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 3.206155819172812e-4
allele num: 6238
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.350598e6

MQ
type: SiteQuality
SIO_000300: 5.917e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

QD
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8789
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6661
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 9.633215326445584e-5
allele num: 41523
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3325
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

DP
type: SiteQuality
SIO_000300: 1.339678e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

QD
type: SiteQuality
SIO_000300: 1.539e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.73e-1

FS
type: SiteQuality
SIO_000300: 1.3806e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.687e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.405291641611545e-5
allele num: 41575
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 507
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6253
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.339819e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.626e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.392e0

VQSLOD
type: SiteQuality
SIO_000300: -1.425e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8800
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.489203276247208e-4
allele num: 6715
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41583
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3350
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.089443294476523e-4
allele num: 9179
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6249
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 505
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.126e0

MQRankSum
type: SiteQuality
SIO_000300: -1.355e0

VQSLOD
type: SiteQuality
SIO_000300: -1.624e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

QD
type: SiteQuality
SIO_000300: 2.938e1

MQ
type: SiteQuality
SIO_000300: 5.604e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.337381e6

FS
type: SiteQuality
SIO_000300: 9.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

GenotypeQuality
all individuals: 839
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41683
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8797
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.08837614279495e-4
allele num: 9188
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.486104919007282e-4
allele num: 6729
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 3.063e1

MQ
type: SiteQuality
SIO_000300: 5.437e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 3.191e0

VQSLOD
type: SiteQuality
SIO_000300: -4.742e-1

DP
type: SiteQuality
SIO_000300: 1.338256e6

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.48544266191325e-4
allele num: 6732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 505
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South Asian
type: Population
allele count: 1
allele frequency: 1.088494611951671e-4
allele num: 9187
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6259
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41609
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 5.617e1

MQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.340658e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.478e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6259
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 505
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9187
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41609
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.617e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.478e1

FS
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.340658e6

MQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41649
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.597444089456869e-4
allele num: 6260
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6776
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.314e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 1.341075e6

FS
type: SiteQuality
SIO_000300: 1.105e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

QD
type: SiteQuality
SIO_000300: 3.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41557
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8783
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3406
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9199
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.866e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6210
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3410
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 515
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.402979694821579e-5
allele num: 41615
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.087e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 1.088494611951671e-4
allele num: 9187
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8784
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.403268445085316e-5
allele num: 41610
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 2.960331557134399e-4
allele num: 6756
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

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

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 510
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3431
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.397621559413062e-5
allele num: 41708
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
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East Asian
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allele frequency: 1.612643122077084e-4
allele num: 6201
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Latino
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Other
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 41950
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East Asian
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allele frequency: 3.228410008071025e-4
allele num: 6195
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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Other
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DP
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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East Asian
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allele frequency: 1.616031027795734e-4
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Other
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South Asian
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allele frequency: 1.092418614813196e-4
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European (Non-Finnish)
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allele frequency: 2.367704510477093e-5
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 3568
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.362613996125313e-5
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South Asian
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East Asian
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African
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Latino
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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variant carriers: 0

South Asian
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Latino
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allele count: 0
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African
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East Asian
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allele frequency: 8.055421298533913e-4
allele num: 6207
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3566
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.363228169679783e-5
allele num: 42315
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Other
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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FS
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DP
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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QD
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
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Latino
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allele count: 0
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9004
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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DP
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1520

Other
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East Asian
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African
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allele frequency: 2.824765971423879e-2
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Latino
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allele frequency: 3.62864576201561e-2
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European (Finnish)
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allele count: 47
allele frequency: 1.553205551883675e-2
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South Asian
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allele frequency: 1.399207528479445e-2
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European (Non-Finnish)
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allele count: 865
allele frequency: 2.422901319290776e-2
allele num: 35701
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MQ
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 451
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.801041987619394e-5
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South Asian
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allele frequency: 2.476473501733531e-4
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Latino
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East Asian
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African
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European (Finnish)
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allele count: 0
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MQRankSum
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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South Asian
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allele frequency: 1.238236750866766e-4
allele num: 8076
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 451
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European (Non-Finnish)
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allele frequency: 2.801041987619394e-5
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East Asian
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African
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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African
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allele num: 6918
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East Asian
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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Latino
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DP
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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QD
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VQSLOD
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GenotypeQuality
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Latino
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European (Finnish)
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African
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 2.435460301997077e-5
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Other
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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African
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East Asian
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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MQ
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QD
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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Latino
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South Asian
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African
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QD
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ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 6889
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.461174964928257e-5
allele num: 40631
num of homozygotes: 0

South Asian
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allele count: 0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 500
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.82e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.259e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.945161100312187e-5
allele num: 33954
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 1.696928559307653e-4
allele num: 5893
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2722
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South Asian
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allele count: 8
allele frequency: 1.15757488062509e-3
allele num: 6911
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Latino
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allele frequency: 0.0e0
allele num: 6655
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.320000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 1.22077e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5893
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6655
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South Asian
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allele count: 0
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Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4910
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33954
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MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.320000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.22077e6

QD
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 25

Latino
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allele count: 37
allele frequency: 5.559729526671675e-3
allele num: 6655
num of homozygotes: 0

African
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allele count: 4
allele frequency: 6.787714237230613e-4
allele num: 5893
num of homozygotes: 0

European (Finnish)
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allele count: 4
allele frequency: 1.469507714915503e-3
allele num: 2722
num of homozygotes: 0

South Asian
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allele count: 22
allele frequency: 3.183330921718999e-3
allele num: 6911
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 1.629327902240326e-3
allele num: 4910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 78
allele frequency: 2.297225658243506e-3
allele num: 33954
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.538071065989848e-3
allele num: 394
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

QD
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 1.22077e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.320000000000001e-2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39674
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3177
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South Asian
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allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 479
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.273e0

DP
type: SiteQuality
SIO_000300: 1.142591e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.234e0

QD
type: SiteQuality
SIO_000300: 2.378e1

GenotypeQuality
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variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6646
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7779
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39956
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5958
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8503
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3180
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 1.160302e6

QD
type: SiteQuality
SIO_000300: 1.708e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

GenotypeQuality
all individuals: 3484
bin: 6.75e1
variant carriers: 0

African
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allele count: 30
allele frequency: 4.801536491677336e-3
allele num: 6248
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8423
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5908
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38989
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3074
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.077706e6

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

QD
type: SiteQuality
SIO_000300: 2.471e1

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38915
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6237
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3072
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.693193362682018e-4
allele num: 5906
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 459
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7284
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.634e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 4.07e0

DP
type: SiteQuality
SIO_000300: 1.072061e6

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5895
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 453
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3039
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 6192
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.580645161290323e-5
allele num: 38750
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.77e-2

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

QD
type: SiteQuality
SIO_000300: 2.882e1

MQ
type: SiteQuality
SIO_000300: 5.878e1

DP
type: SiteQuality
SIO_000300: 1.036676e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8263
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36874
num of homozygotes: 0

African
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allele frequency: 1.697504668137837e-4
allele num: 5891
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 419
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DP
type: SiteQuality
SIO_000300: 9.49829e5

MQRankSum
type: SiteQuality
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MQ
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FS
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36753
num of homozygotes: 0

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

East Asian
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South Asian
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Latino
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allele frequency: 1.213739531496541e-4
allele num: 8239
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 423
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 44972
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Other
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allele frequency: 0.0e0
allele num: 577
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3795
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 4
allele frequency: 4.319654427645788e-4
allele num: 9260
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.667455e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3793
num of homozygotes: 0

Latino
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allele num: 8911
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Other
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African
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allele frequency: 2.477086945751796e-4
allele num: 8074
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South Asian
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European (Non-Finnish)
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East Asian
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allele frequency: 1.578282828282828e-4
allele num: 6336
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InbreedingCoeff
type: SiteQuality
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MQ
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele num: 8911
num of homozygotes: 0

African
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Other
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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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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VQSLOD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.36e-1

DP
type: SiteQuality
SIO_000300: 1.68103e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3885
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 587
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.188614825676829e-5
allele num: 45691
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6431
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9360
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.607e1

DP
type: SiteQuality
SIO_000300: 1.773727e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.671e0

VQSLOD
type: SiteQuality
SIO_000300: -8.964e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.108156028368794e-4
allele num: 9024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 587
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.185171426698424e-5
allele num: 45763
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8161
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6439
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3899
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.779903e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.449e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8199
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9058
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3945
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.545117428924598e-4
allele num: 6472
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46046
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.68e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.812591e6

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.301e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4087
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46803
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9157
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.921e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.685e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.366e1

DP
type: SiteQuality
SIO_000300: 1.870377e6

MQRankSum
type: SiteQuality
SIO_000300: -8.05e-1

FS
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6565
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9177
num of homozygotes: 0

African
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
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46956
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 3.863e0

QD
type: SiteQuality
SIO_000300: 1.39e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.878136e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4209
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47380
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.083893344894862e-4
allele num: 9226
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8379
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6597
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9799
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.396e0

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.614e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 1.905634e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4211
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9225
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.019783805833163e-4
allele num: 9806
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47375
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.548e0

MQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

QD
type: SiteQuality
SIO_000300: 2.901e1

FS
type: SiteQuality
SIO_000300: 2.561e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.72e-2

DP
type: SiteQuality
SIO_000300: 1.907118e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8357
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.024065540194572e-4
allele num: 9765
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.90112e6

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

QD
type: SiteQuality
SIO_000300: 1.245e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.052e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3901
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.524434005350036e-5
allele num: 45981
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.42e-1

FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8177
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.185840127653063e-5
allele num: 45749
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 9418
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 585
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 8991
num of homozygotes: 0

QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 567
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3690
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8021
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.241549358916883e-5
allele num: 44612
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8484
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African
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allele count: 5
allele frequency: 6.459113809585325e-4
allele num: 7741
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42741
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 541
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele frequency: 1.170548987475126e-4
allele num: 8543
num of homozygotes: 0

European (Non-Finnish)
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African
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3141
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8497
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East Asian
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allele frequency: 1.748863238894718e-4
allele num: 5718
num of homozygotes: 0

Latino
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allele frequency: 1.231072263941894e-4
allele num: 8123
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40657
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.854e1

DP
type: SiteQuality
SIO_000300: 1.477482e6

FS
type: SiteQuality
SIO_000300: 4.109e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.48e-1

GenotypeQuality
all individuals: 5197
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7597
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 473
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.882884579175297e-4
allele num: 5311
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.24e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

DP
type: SiteQuality
SIO_000300: 1.341426e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.334e0

MQ
type: SiteQuality
SIO_000300: 5.861e1

GenotypeQuality
all individuals: 314
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2095
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.02535245356084e-5
allele num: 33054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7435
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6716
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.28e0

MQ
type: SiteQuality
SIO_000300: 5.742e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

FS
type: SiteQuality
SIO_000300: 3.565e0

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

DP
type: SiteQuality
SIO_000300: 1.247289e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

GenotypeQuality
all individuals: 2969
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6975
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 373
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5805
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1647
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.492595697122101e-5
allele num: 28632
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.338e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

DP
type: SiteQuality
SIO_000300: 1.213918e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.373e0

GenotypeQuality
all individuals: 1298
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6975
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5805
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 373
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1647
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.338e1

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.373e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

DP
type: SiteQuality
SIO_000300: 1.213918e6

GenotypeQuality
all individuals: 2506
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9259
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.242152466367713e-4
allele num: 4460
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.36e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.206503e6

QD
type: SiteQuality
SIO_000300: 2.863e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1166
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4465
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.964129135113592e-5
allele num: 10036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.100090303883067e-5
allele num: 47617
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

DP
type: SiteQuality
SIO_000300: 2.208269e6

QD
type: SiteQuality
SIO_000300: 1.687e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

GenotypeQuality
all individuals: 757
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4469
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6613
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8461
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.09643605870021e-5
allele num: 47700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10049
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.514e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.178e0

DP
type: SiteQuality
SIO_000300: 2.252705e6

VQSLOD
type: SiteQuality
SIO_000300: -3.636e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.539e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

QD
type: SiteQuality
SIO_000300: 1.023e1

GenotypeQuality
all individuals: 1230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13776
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8493
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6629
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075268817204301e-4
allele num: 9300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47912
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.31e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.898e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.289021e6

GenotypeQuality
all individuals: 13776
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2571
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508295625942685e-4
allele num: 6630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087116231502932e-5
allele num: 47913
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10103
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

DP
type: SiteQuality
SIO_000300: 2.2898e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.63e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.846e0

QD
type: SiteQuality
SIO_000300: 1.775e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 1224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24478
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 663
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.056922844632342e-3
allele num: 6623
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10047
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9277
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47737
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.345e1

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 2.262909e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.274e0

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.62e-2

GenotypeQuality
all individuals: 1344
bin: 3.75e1
variant carriers: 23

GenotypeQuality
all individuals: 930
bin: 4.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1721
bin: 2.75e1
variant carriers: 12

South Asian
type: Population
allele count: 4
allele frequency: 4.070418235473695e-4
allele num: 9827
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 7.704160246533128e-4
allele num: 6490
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 4.106280193236715e-3
allele num: 8280
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 4.975124378109453e-3
allele num: 603
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.099384344766931e-3
allele num: 9096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4371
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 322
allele frequency: 6.946691692015619e-3
allele num: 46353
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 2.22e0