X-50053411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053411
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053411
    reference: chr 0
allele count: 4
allele frequency: 4.917266983010843e-5
allele num: 81346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2242T>C
  hgvsp: ENSP00000276014.7:p.Ser748Pro
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2242T>C
  hgvsp: ENSP00000365210.1:p.Ser748Pro
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2126T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21524T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21524T>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 9569
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  variant carriers: 0
hgvs: p.Ser748Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-50053413-T-TTTAAAGAAGAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053413
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053425
    reference: chr 0
allele count: 1
allele frequency: 1.233425840271354e-5
allele num: 81075
alternate allele: TTTAAAGAAGAAG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsp: ENSP00000365210.1:p.Leu749_Lys752dup
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsp: ENSP00000276014.7:p.Leu749_Lys752dup
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Leu749_Lys752dup
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-50053423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053423
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053423
    reference: chr 0
allele count: 1
allele frequency: 1.254248767700586e-5
allele num: 79729
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2114A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2254A>G
  hgvsp: ENSP00000276014.7:p.Lys752Glu
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2254A>G
  hgvsp: ENSP00000365210.1:p.Lys752Glu
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21536A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21536A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Lys752Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-50053427-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053427
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053427
    reference: chr 0
allele count: 1
allele frequency: 1.26519819329698e-5
allele num: 79039
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2258C>A
  hgvsp: ENSP00000365210.1:p.Ser753Tyr
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21540C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2110C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21540C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2258C>A
  hgvsp: ENSP00000276014.7:p.Ser753Tyr
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ser753Tyr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

X-50053427-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053427
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053427
    reference: chr 0
allele count: 3
allele frequency: 3.79559457989094e-5
allele num: 79039
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21540C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21540C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2258C>G
  hgvsp: ENSP00000276014.7:p.Ser753Cys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2110C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2258C>G
  hgvsp: ENSP00000365210.1:p.Ser753Cys
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11950
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 369
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 916
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genotype quality: GenotypeQuality
  all individuals: 2462
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2991
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser753Cys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

X-50053429-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053429
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053429
    reference: chr 0
allele count: 1
allele frequency: 1.270196118280662e-5
allele num: 78728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2260A>G
  hgvsp: ENSP00000276014.7:p.Thr754Ala
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21542A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21542A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2260A>G
  hgvsp: ENSP00000365210.1:p.Thr754Ala
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2108A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
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  variant carriers: 0
hgvs: p.Thr754Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

X-50053430-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053430
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053430
    reference: chr 0
allele count: 1
allele frequency: 1.272313192615494e-5
allele num: 78597
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2261C>A
  hgvsp: ENSP00000276014.7:p.Thr754Asn
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2261C>A
  hgvsp: ENSP00000365210.1:p.Thr754Asn
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21543C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2107C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21543C>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
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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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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.Thr754Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-50053433-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053433
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053433
    reference: chr 0
allele count: 1
allele frequency: 1.277906278353545e-5
allele num: 78253
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2104C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21546C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2264C>A
  hgvsp: ENSP00000365210.1:p.Ser755Tyr
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21546C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2264C>A
  hgvsp: ENSP00000276014.7:p.Ser755Tyr
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
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: 533
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  variant carriers: 0
hgvs: p.Ser755Tyr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

X-50053444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053444
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053444
    reference: chr 0
allele count: 1
allele frequency: 1.295554950963245e-5
allele num: 77187
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21557G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2275G>A
  hgvsp: ENSP00000276014.7:p.Val759Met
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2093G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2275G>A
  hgvsp: ENSP00000365210.1:p.Val759Met
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21557G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
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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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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  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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  bin: 6.75e1
  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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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14119
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val759Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

X-50053447-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053447
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053447
    reference: chr 0
allele count: 1
allele frequency: 1.301896863730455e-5
allele num: 76811
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2090T>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21560T>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21560T>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2278T>A
  hgvsp: ENSP00000365210.1:p.Phe760Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2278T>A
  hgvsp: ENSP00000276014.7:p.Phe760Ile
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8803
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 118
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 55
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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
  all individuals: 116
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genotype quality: GenotypeQuality
  all individuals: 26386
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 473
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 778
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
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  variant carriers: 0
hgvs: p.Phe760Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

X-50053474-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053474
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053474
    reference: chr 0
allele count: 1
allele frequency: 1.331717516080489e-5
allele num: 75091
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21587A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2305A>G
  hgvsp: ENSP00000276014.7:p.Asn769Asp
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21587A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2305A>G
  hgvsp: ENSP00000365210.1:p.Asn769Asp
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2063A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18325
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
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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: 1
genotype depth: GenotypeDepth
  all individuals: 3
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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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genotype depth: GenotypeDepth
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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
  all individuals: 24381
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  variant carriers: 0
hgvs: p.Asn769Asp
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

X-50053492-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053492
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053492
    reference: chr 0
allele count: 3
allele frequency: 4.022634020756792e-5
allele num: 74578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21605G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21605G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2323G>A
  hgvsp: ENSP00000276014.7:p.Glu775Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2323G>A
  hgvsp: ENSP00000365210.1:p.Glu775Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2045G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 8872
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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 quality: GenotypeQuality
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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: 2991
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu775Lys
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: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

X-50053500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053500
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053500
    reference: chr 0
allele count: 51
allele frequency: 6.848855166856913e-4
allele num: 74465
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2037C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2331C>T
  hgvsp: ENST00000276014.7:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2331C>T
  hgvsp: ENST00000376042.1:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21613C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21613C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 17796
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3026
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe777Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-50053505-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053505
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053505
    reference: chr 0
allele count: 1
allele frequency: 1.340231055834026e-5
allele num: 74614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21618A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21618A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2336A>G
  hgvsp: ENSP00000276014.7:p.Asn779Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2336A>G
  hgvsp: ENSP00000365210.1:p.Asn779Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-2032A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
genotype quality: GenotypeQuality
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  bin: 5.25e1
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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: 1.75e1
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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
  all individuals: 775
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genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn779Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

X-50053539-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053539
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053539
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 77516
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2370C>T
  hgvsp: ENST00000376042.1:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2370C>T
  hgvsp: ENST00000276014.7:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21652C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21652C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1998C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 352
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hgvs: p.Ser790Ser
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

X-50053544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053544
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053544
    reference: chr 0
allele count: 7
allele frequency: 8.972748481041865e-5
allele num: 78014
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2375C>T
  hgvsp: ENSP00000365210.1:p.Ala792Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2375C>T
  hgvsp: ENSP00000276014.7:p.Ala792Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21657C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21657C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1993C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26628
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 595
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala792Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-50053545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053545
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053545
    reference: chr 0
allele count: 2
allele frequency: 2.548225161175241e-5
allele num: 78486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2376G>A
  hgvsp: ENST00000276014.7:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1992G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21658G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21658G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2376G>A
  hgvsp: ENST00000376042.1:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8177
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12064
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 18
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genotype depth: GenotypeDepth
  all individuals: 27488
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2431
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genotype quality: GenotypeQuality
  all individuals: 698
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genotype quality: GenotypeQuality
  all individuals: 572
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 2913
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genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 231
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genotype quality: GenotypeQuality
  all individuals: 434
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genotype quality: GenotypeQuality
  all individuals: 609
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genotype quality: GenotypeQuality
  all individuals: 10906
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala792Ala
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

X-50053553-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053553
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053553
    reference: chr 0
allele count: 1
allele frequency: 1.254894086939062e-5
allele num: 79688
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2384A>G
  hgvsp: ENSP00000276014.7:p.Glu795Gly
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1984A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21666A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2384A>G
  hgvsp: ENSP00000365210.1:p.Glu795Gly
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21666A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
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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: 6004
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
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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 quality: GenotypeQuality
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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: 342
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 332
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9480
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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
  all individuals: 1036
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genotype quality: GenotypeQuality
  all individuals: 436
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
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  variant carriers: 0
hgvs: p.Glu795Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-50053557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053557
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053557
    reference: chr 0
allele count: 1
allele frequency: 1.245298996289009e-5
allele num: 80302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21670C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2388C>T
  hgvsp: ENST00000276014.7:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1980C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2388C>T
  hgvsp: ENST00000376042.1:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21670C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30718
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
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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
  all individuals: 5434
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 61
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hgvs: p.Thr796Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-50053558-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053558
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053558
    reference: chr 0
allele count: 1
allele frequency: 1.243301712026457e-5
allele num: 80431
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2389C>A
  hgvsp: ENSP00000365210.1:p.Leu797Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1979C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2389C>A
  hgvsp: ENSP00000276014.7:p.Leu797Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21671C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21671C>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu797Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

X-50053575-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053575
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053575
    reference: chr 0
allele count: 1
allele frequency: 1.218353273715246e-5
allele num: 82078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21688G>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1962G>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2406G>T
  hgvsp: ENSP00000276014.7:p.Leu802Phe
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2406G>T
  hgvsp: ENSP00000365210.1:p.Leu802Phe
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21688G>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
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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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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu802Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-50053596-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053596
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053596
    reference: chr 0
allele count: 1
allele frequency: 1.206025302410845e-5
allele num: 82917
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2427C>A
  hgvsp: ENSP00000276014.7:p.Ser809Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21709C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1941C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2427C>A
  hgvsp: ENSP00000365210.1:p.Ser809Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21709C>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  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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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1011
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser809Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-50053610-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053610
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053610
    reference: chr 0
allele count: 1
allele frequency: 1.206127125799059e-5
allele num: 82910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21723C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2441C>G
  hgvsp: ENSP00000365210.1:p.Ala814Gly
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21723C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2441C>G
  hgvsp: ENSP00000276014.7:p.Ala814Gly
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1927C>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
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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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  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Ala814Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

X-50053642-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053642
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053642
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 82193
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2473G>C
  hgvsp: ENSP00000365210.1:p.Ala825Pro
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21755G>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2473G>C
  hgvsp: ENSP00000276014.7:p.Ala825Pro
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21755G>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1895G>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  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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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala825Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

X-50053657-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053657
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053657
    reference: chr 0
allele count: 1
allele frequency: 1.222150251151877e-5
allele num: 81823
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21770C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1880C>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2488C>G
  hgvsp: ENSP00000276014.7:p.Pro830Ala
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2488C>G
  hgvsp: ENSP00000365210.1:p.Pro830Ala
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21770C>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 7.75e1
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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
  all individuals: 227
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  variant carriers: 0
hgvs: p.Pro830Ala
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: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

X-50053661-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053661
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053661
    reference: chr 0
allele count: 1
allele frequency: 1.222493887530562e-5
allele num: 81800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1876T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21774T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2492T>C
  hgvsp: ENSP00000365210.1:p.Leu831Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2492T>C
  hgvsp: ENSP00000276014.7:p.Leu831Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21774T>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Leu831Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

X-50053667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053667
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053667
    reference: chr 0
allele count: 4
allele frequency: 4.894223592604828e-5
allele num: 81729
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2498T>C
  hgvsp: ENSP00000365210.1:p.Leu833Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2498T>C
  hgvsp: ENSP00000276014.7:p.Leu833Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21780T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21780T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1870T>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Leu833Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

X-50053668-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053668
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053668
    reference: chr 0
allele count: 1
allele frequency: 1.225009800078401e-5
allele num: 81632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21781G>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1869G>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21781G>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2499G>C
  hgvsp: ENSP00000276014.7:p.Leu833Phe
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
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  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2499G>C
  hgvsp: ENSP00000365210.1:p.Leu833Phe
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8502
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3010
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu833Phe
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

X-50053675-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053675
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053675
    reference: chr 0
allele count: 1
allele frequency: 1.226753030079984e-5
allele num: 81516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21788G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21788G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1862G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2506G>A
  hgvsp: ENSP00000276014.7:p.Glu836Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2506G>A
  hgvsp: ENSP00000365210.1:p.Glu836Lys
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
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genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8642
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2734
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu836Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

X-50053685-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053685
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053685
    reference: chr 0
allele count: 1
allele frequency: 1.230405787828826e-5
allele num: 81274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21798C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2516C>T
  hgvsp: ENSP00000276014.7:p.Thr839Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2516C>T
  hgvsp: ENSP00000365210.1:p.Thr839Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1852C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21798C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
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genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Thr839Ile
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-50053686-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053686
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053686
    reference: chr 0
allele count: 3
allele frequency: 3.683196031970142e-5
allele num: 81451
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2517T>C
  hgvsp: ENST00000276014.7:c.2517T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2517T>C
  hgvsp: ENST00000376042.1:c.2517T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21799T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21799T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1851T>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24486
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8827
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 259
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  variant carriers: 0
hgvs: p.Thr839Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

X-50053690-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053690
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053690
    reference: chr 0
allele count: 1
allele frequency: 1.229271410834798e-5
allele num: 81349
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1847A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2521A>C
  hgvsp: ENSP00000276014.7:p.Lys841Gln
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21803A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2521A>C
  hgvsp: ENSP00000365210.1:p.Lys841Gln
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21803A>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5232
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
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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 quality: GenotypeQuality
  all individuals: 2940
  bin: 2.75e1
  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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  variant carriers: 0
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: 275
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys841Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-50053697-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053697
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053697
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 81216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21810C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2528C>T
  hgvsp: ENSP00000276014.7:p.Ala843Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1840C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21810C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2528C>T
  hgvsp: ENSP00000365210.1:p.Ala843Val
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23802
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
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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: 88
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8921
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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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genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
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: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2480
  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.25e1
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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
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala843Val
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

X-50053701-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053701
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053701
    reference: chr 0
allele count: 8
allele frequency: 9.863027209626315e-5
allele num: 81111
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2532C>T
  hgvsp: ENST00000376042.1:c.2532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21814C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21814C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1836C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2532C>T
  hgvsp: ENST00000276014.7:c.2532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
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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
  all individuals: 272
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 2
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
  all individuals: 1925
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
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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: 8.25e1
  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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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8731
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 144
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val844Val
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

X-50053706-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053706
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053706
    reference: chr 0
allele count: 15
allele frequency: 1.846858493702213e-4
allele num: 81219
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2537A>G
  hgvsp: ENSP00000276014.7:p.Lys846Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21819A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2537A>G
  hgvsp: ENSP00000365210.1:p.Lys846Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21819A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1831A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 67
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  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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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: 2882
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys846Arg
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: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-50053738-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053738
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053738
    reference: chr 0
allele count: 188
allele frequency: 2.310717797443461e-3
allele num: 81360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2569A>C
  hgvsp: ENSP00000276014.7:p.Lys857Gln
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1799A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21851A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2569A>C
  hgvsp: ENSP00000365210.1:p.Lys857Gln
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21851A>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24029
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  variant carriers: 20
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: 20
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 7.5e0
  variant carriers: 3
hgvs: p.Lys857Gln
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-50053745-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053745
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053745
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 81454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21858C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21858C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2576C>A
  hgvsp: ENSP00000276014.7:p.Thr859Asn
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1792C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2576C>A
  hgvsp: ENSP00000365210.1:p.Thr859Asn
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 24593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13915
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genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
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genotype depth: GenotypeDepth
  all individuals: 2012
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
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genotype depth: GenotypeDepth
  all individuals: 23
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34412
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genotype quality: GenotypeQuality
  all individuals: 2368
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
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genotype quality: GenotypeQuality
  all individuals: 60
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8233
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr859Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD

X-50053774-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053774
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053774
    reference: chr 0
allele count: 4
allele frequency: 4.811046161987924e-5
allele num: 83142
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2605G>A
  hgvsp: ENSP00000365210.1:p.Glu869Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1763G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21887G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21887G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2605G>A
  hgvsp: ENSP00000276014.7:p.Glu869Lys
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15779
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
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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
  all individuals: 13
  bin: 6.75e1
  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
  all individuals: 32
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 457
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 460
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42435
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
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genotype quality: GenotypeQuality
  all individuals: 79
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genotype quality: GenotypeQuality
  all individuals: 683
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genotype quality: GenotypeQuality
  all individuals: 6009
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu869Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

X-50053776-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053776
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053776
    reference: chr 0
allele count: 1
allele frequency: 1.201013655525263e-5
allele num: 83263
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21889G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2607G>A
  hgvsp: ENST00000376042.1:c.2607G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2607G>A
  hgvsp: ENST00000276014.7:c.2607G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21889G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1761G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
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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 quality: GenotypeQuality
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  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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  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
  all individuals: 85
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  variant carriers: 0
hgvs: p.Glu869Glu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

X-50053782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053782
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053782
    reference: chr 0
allele count: 1
allele frequency: 1.19293306452575e-5
allele num: 83827
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21895G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2613G>A
  hgvsp: ENST00000376042.1:c.2613G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21895G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1755G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2613G>A
  hgvsp: ENST00000276014.7:c.2613G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
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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
  all individuals: 3893
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44749
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3325
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu871Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

X-50053795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053795
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053795
    reference: chr 0
allele count: 1
allele frequency: 1.182354540832614e-5
allele num: 84577
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1742C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2626C>T
  hgvsp: ENSP00000276014.7:p.Arg876Ter
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21908C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21908C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2626C>T
  hgvsp: ENSP00000365210.1:p.Arg876Ter
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
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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
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46607
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg876Ter
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

X-50053796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053796
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053796
    reference: chr 0
allele count: 84
allele frequency: 9.918526390364859e-4
allele num: 84690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21909G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1741G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2627G>A
  hgvsp: ENSP00000276014.7:p.Arg876Gln
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21909G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2627G>A
  hgvsp: ENSP00000365210.1:p.Arg876Gln
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 142
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  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17163
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 310
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  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 33510
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
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  variant carriers: 9
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 61
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  variant carriers: 8
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 11
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  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
  all individuals: 668
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 74
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 47176
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 171
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg876Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

X-50053809-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053809
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053809
    reference: chr 0
allele count: 1
allele frequency: 1.17057639181533e-5
allele num: 85428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21922G>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21922G>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2640G>T
  hgvsp: ENSP00000365210.1:p.Leu880Phe
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2640G>T
  hgvsp: ENSP00000276014.7:p.Leu880Phe
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1728G>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34545
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Leu880Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-50053810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053810
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053810
    reference: chr 0
allele count: 3
allele frequency: 3.510208857427017e-5
allele num: 85465
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2641T>C
  hgvsp: ENSP00000365210.1:p.Trp881Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1727T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21923T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21923T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2641T>C
  hgvsp: ENSP00000276014.7:p.Trp881Arg
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
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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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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3660
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp881Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

X-50053821-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053821
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053821
    reference: chr 0
allele count: 1
allele frequency: 1.165134514779731e-5
allele num: 85827
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2652C>A
  hgvsp: ENST00000276014.7:c.2652C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21934C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2652C>A
  hgvsp: ENST00000376042.1:c.2652C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1716C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21934C>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 7.5e0
  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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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
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genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  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: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49358
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro884Pro
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

X-50053874-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053874
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053874
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 86664
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2705C>A
  hgvsp: ENSP00000365210.1:p.Pro902His
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2705C>A
  hgvsp: ENSP00000276014.7:p.Pro902His
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21987C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1663C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21987C>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 242
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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: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 633
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro902His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-50053880-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053880
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053880
    reference: chr 0
allele count: 1
allele frequency: 1.152870647913304e-5
allele num: 86740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+21993T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1657T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2711T>C
  hgvsp: ENSP00000276014.7:p.Ile904Thr
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+21993T>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2711T>C
  hgvsp: ENSP00000365210.1:p.Ile904Thr
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  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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  bin: 1.25e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 171
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genotype quality: GenotypeQuality
  all individuals: 3881
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  variant carriers: 0
hgvs: p.Ile904Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

X-50053887-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053887
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053887
    reference: chr 0
allele count: 92
allele frequency: 1.059346429311655e-3
allele num: 86846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22000A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2718A>G
  hgvsp: ENST00000276014.7:c.2718A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2718A>G
  hgvsp: ENST00000376042.1:c.2718A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1650A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22000A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 55
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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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  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 907
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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: 5
genotype depth: GenotypeDepth
  all individuals: 34376
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 6
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 10
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1188
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 406
  bin: 9.75e1
  variant carriers: 81
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50962
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys906Lys
num of homozygotes: 1
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-50053921-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053921
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053921
    reference: chr 0
allele count: 1
allele frequency: 1.144701747959569e-5
allele num: 87359
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1616A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2752A>C
  hgvsp: ENSP00000365210.1:p.Met918Leu
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22034A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22034A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2752A>C
  hgvsp: ENSP00000276014.7:p.Met918Leu
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21020
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 438
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53241
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  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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genotype quality: GenotypeQuality
  all individuals: 112
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4153
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genotype quality: GenotypeQuality
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met918Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

X-50053921-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053921
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053921
    reference: chr 0
allele count: 1
allele frequency: 1.144701747959569e-5
allele num: 87359
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1616A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22034A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2752A>G
  hgvsp: ENSP00000365210.1:p.Met918Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22034A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2752A>G
  hgvsp: ENSP00000276014.7:p.Met918Val
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
hgvs: p.Met918Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

X-50053923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053923
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053923
    reference: chr 0
allele count: 1
allele frequency: 1.14432187485696e-5
allele num: 87388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22036G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2754G>A
  hgvsp: ENSP00000365210.1:p.Met918Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2754G>A
  hgvsp: ENSP00000276014.7:p.Met918Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22036G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1614G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Met918Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

X-50053930-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053930
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053930
    reference: chr 0
allele count: 1
allele frequency: 1.143484425742121e-5
allele num: 87452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22043A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22043A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2761A>G
  hgvsp: ENSP00000365210.1:p.Ile921Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2761A>G
  hgvsp: ENSP00000276014.7:p.Ile921Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1607A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21179
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 53546
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile921Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

X-50053934-A-ATGAGGCAGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053934
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053943
    reference: chr 0
allele count: 1
allele frequency: 1.143301397114307e-5
allele num: 87466
alternate allele: ATGAGGCAGT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsp: ENSP00000365210.1:p.Glu923_Val925dup
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsp: ENSP00000276014.7:p.Glu923_Val925dup
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53627
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu923_Val925dup
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

X-50053944-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053944
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053944
    reference: chr 0
allele count: 1
allele frequency: 1.142752662613704e-5
allele num: 87508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1593C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22057C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22057C>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2775C>A
  hgvsp: ENST00000376042.1:c.2775C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2775C>A
  hgvsp: ENST00000276014.7:c.2775C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53688
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val925Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

X-50053950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053950
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053950
    reference: chr 0
allele count: 6
allele frequency: 6.854087892253739e-5
allele num: 87539
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2781C>T
  hgvsp: ENST00000276014.7:c.2781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2781C>T
  hgvsp: ENST00000376042.1:c.2781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1587C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22063C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22063C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
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genotype depth: GenotypeDepth
  all individuals: 15
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genotype depth: GenotypeDepth
  all individuals: 77
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genotype depth: GenotypeDepth
  all individuals: 32
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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: 62
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genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 53744
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 31
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 66
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genotype quality: GenotypeQuality
  all individuals: 864
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 179
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genotype quality: GenotypeQuality
  all individuals: 15
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
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  variant carriers: 0
hgvs: p.Phe927Phe
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: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-50053951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053951
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053951
    reference: chr 0
allele count: 14
allele frequency: 1.599287174859206e-4
allele num: 87539
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2782G>A
  hgvsp: ENSP00000276014.7:p.Glu928Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1586G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2782G>A
  hgvsp: ENSP00000365210.1:p.Glu928Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22064G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22064G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35133
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 131
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21410
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 12
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4255
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu928Lys
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

X-50053963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053963
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053963
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2794G>A
  hgvsp: ENSP00000276014.7:p.Ala932Thr
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22076G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1574G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22076G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2794G>A
  hgvsp: ENSP00000365210.1:p.Ala932Thr
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35086
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
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genotype depth: GenotypeDepth
  all individuals: 25
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 565
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala932Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

X-50053968-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053968
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053968
    reference: chr 0
allele count: 1
allele frequency: 1.142100093652208e-5
allele num: 87558
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2799G>A
  hgvsp: ENST00000376042.1:c.2799G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22081G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22081G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1569G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2799G>A
  hgvsp: ENST00000276014.7:c.2799G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21529
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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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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: 52
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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: 354
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 22
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53817
  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu933Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

X-50053993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053993
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053993
    reference: chr 0
allele count: 1
allele frequency: 1.141839274703693e-5
allele num: 87578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22106G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2824G>A
  hgvsp: ENSP00000365210.1:p.Glu942Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22106G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2824G>A
  hgvsp: ENSP00000276014.7:p.Glu942Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1544G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
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  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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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Glu942Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-50053995-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050053995
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050053995
    reference: chr 0
allele count: 3
allele frequency: 3.42583076396026e-5
allele num: 87570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22108G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2826G>A
  hgvsp: ENST00000276014.7:c.2826G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22108G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2826G>A
  hgvsp: ENST00000376042.1:c.2826G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1542G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
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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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  bin: 6.25e1
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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 quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53788
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu942Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

X-50054006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054006
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054006
    reference: chr 0
allele count: 2
allele frequency: 2.283939338571168e-5
allele num: 87568
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2837A>G
  hgvsp: ENSP00000365210.1:p.Lys946Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2837A>G
  hgvsp: ENSP00000276014.7:p.Lys946Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22119A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1531A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22119A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
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genotype depth: GenotypeDepth
  all individuals: 54
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53695
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genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys946Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-50054010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054010
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054010
    reference: chr 0
allele count: 1
allele frequency: 1.141917507879231e-5
allele num: 87572
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2841G>A
  hgvsp: ENST00000376042.1:c.2841G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2841G>A
  hgvsp: ENST00000276014.7:c.2841G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22123G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1527G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22123G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21694
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53778
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 564
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 46
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genotype quality: GenotypeQuality
  all individuals: 4288
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu947Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS

X-50054037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054037
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054037
    reference: chr 0
allele count: 1
allele frequency: 1.141865351237782e-5
allele num: 87576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2868C>T
  hgvsp: ENST00000276014.7:c.2868C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1500C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22150C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22150C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2868C>T
  hgvsp: ENST00000376042.1:c.2868C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21760
  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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  bin: 1.25e1
  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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  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 quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  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
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr956Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

X-50054039-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054039
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054039
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87560
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22152A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22152A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2870A>G
  hgvsp: ENSP00000365210.1:p.Tyr957Cys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2870A>G
  hgvsp: ENSP00000276014.7:p.Tyr957Cys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1498A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4275
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr957Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

X-50054044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054044
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054044
    reference: chr 0
allele count: 1
allele frequency: 1.14187838995147e-5
allele num: 87575
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22157G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2875G>A
  hgvsp: ENSP00000365210.1:p.Glu959Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1493G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2875G>A
  hgvsp: ENSP00000276014.7:p.Glu959Lys
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22157G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 10
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34734
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
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genotype depth: GenotypeDepth
  all individuals: 6
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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: 53796
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genotype quality: GenotypeQuality
  all individuals: 35
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genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 22
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 866
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 575
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genotype quality: GenotypeQuality
  all individuals: 11
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu959Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-50054045-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054045
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054045
    reference: chr 0
allele count: 1
allele frequency: 1.141865351237782e-5
allele num: 87576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1492A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22158A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2876A>C
  hgvsp: ENSP00000276014.7:p.Glu959Ala
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2876A>C
  hgvsp: ENSP00000365210.1:p.Glu959Ala
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22158A>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34739
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 328
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 11
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genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
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genotype quality: GenotypeQuality
  all individuals: 53798
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genotype quality: GenotypeQuality
  all individuals: 574
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu959Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-50054051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054051
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054051
    reference: chr 0
allele count: 3
allele frequency: 3.425635169854411e-5
allele num: 87575
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2882C>T
  hgvsp: ENSP00000365210.1:p.Thr961Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1486C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2882C>T
  hgvsp: ENSP00000276014.7:p.Thr961Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22164C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22164C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34716
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 21779
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 18
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hgvs: p.Thr961Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-50054074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054074
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054074
    reference: chr 0
allele count: 1
allele frequency: 1.141721945037505e-5
allele num: 87587
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2905C>T
  hgvsp: ENSP00000276014.7:p.Pro969Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22187C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1463C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2905C>T
  hgvsp: ENSP00000365210.1:p.Pro969Ser
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22187C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
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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
  all individuals: 135
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genotype depth: GenotypeDepth
  all individuals: 24
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21820
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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: 78
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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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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53755
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro969Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-50054098-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054098
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054098
    reference: chr 0
allele count: 1
allele frequency: 1.141643738654915e-5
allele num: 87593
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22211G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2929G>A
  hgvsp: ENSP00000365210.1:p.Val977Met
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22211G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1439G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2929G>A
  hgvsp: ENSP00000276014.7:p.Val977Met
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
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genotype depth: GenotypeDepth
  all individuals: 125
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 12
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  variant carriers: 0
hgvs: p.Val977Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

X-50054100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054100
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054100
    reference: chr 0
allele count: 1
allele frequency: 1.141734980476332e-5
allele num: 87586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1437G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2931G>A
  hgvsp: ENST00000376042.1:c.2931G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2931G>A
  hgvsp: ENST00000276014.7:c.2931G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22213G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22213G>A
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
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genotype depth: GenotypeDepth
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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: 21834
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 176
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  variant carriers: 0
hgvs: p.Val977Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-50054106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054106
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054106
    reference: chr 0
allele count: 1
allele frequency: 1.141695875052804e-5
allele num: 87589
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2937C>T
  hgvsp: ENST00000376042.1:c.2937C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1431C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22219C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22219C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2937C>T
  hgvsp: ENST00000276014.7:c.2937C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
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genotype depth: GenotypeDepth
  all individuals: 13
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 71
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hgvs: p.Ser979Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

X-50054108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054108
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054108
    reference: chr 0
allele count: 1
allele frequency: 1.141721945037505e-5
allele num: 87587
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1429C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2939C>T
  hgvsp: ENSP00000276014.7:p.Thr980Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2939C>T
  hgvsp: ENSP00000365210.1:p.Thr980Ile
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22221C>T
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22221C>T
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34627
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr980Ile
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-50054110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054110
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054110
    reference: chr 0
allele count: 1
allele frequency: 1.141839274703693e-5
allele num: 87578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1427G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22223G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2941G>A
  hgvsp: ENSP00000365210.1:p.Ala981Thr
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22223G>A
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2941G>A
  hgvsp: ENSP00000276014.7:p.Ala981Thr
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53709
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala981Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

X-50054137-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054137
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054137
    reference: chr 0
allele count: 1
allele frequency: 1.141891428962934e-5
allele num: 87574
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2968A>C
  hgvsp: ENSP00000365210.1:p.Ser990Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22250A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2968A>C
  hgvsp: ENSP00000276014.7:p.Ser990Arg
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1400A>C
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22250A>C
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53767
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser990Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

X-50054140-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24050054140
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24050054140
    reference: chr 0
allele count: 25
allele frequency: 2.854370040532055e-4
allele num: 87585
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000276014
  ensembl transcript: ENST00000276014
  gene symbol: CCNB3
  hgvsc: ENST00000276014.7:c.2971A>G
  hgvsp: ENSP00000276014.7:p.Ile991Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365206
  ensembl transcript: ENST00000376038
  gene symbol: CCNB3
  hgvsc: ENST00000376038.1:c.204+22253A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000338682
  ensembl transcript: ENST00000348603
  gene symbol: CCNB3
  hgvsc: ENST00000348603.2:c.204+22253A>G
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000365210
  ensembl transcript: ENST00000376042
  gene symbol: CCNB3
  hgvsc: ENST00000376042.1:c.2971A>G
  hgvsp: ENSP00000365210.1:p.Ile991Val
  variant of: http://identifiers.org/hgnc/18709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147082
  ensembl protein: ENSP00000431645
  ensembl transcript: ENST00000476167
  gene symbol: CCNB3
  hgvsc: ENST00000476167.1:c.*-1397A>G
  variant of: http://identifiers.org/hgnc/18709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile991Val
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 5.068423720223011e-4
allele num: 7892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6175
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44475
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9005
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8925
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 1.2308e1

QD
type: SiteQuality
SIO_000300: 1.362e1

VQSLOD
type: SiteQuality
SIO_000300: 3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.264878e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

GenotypeQuality
all individuals: 789
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38568
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8897
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4275
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.114827201783724e-4
allele num: 8970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.393e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.255185e6

MQ
type: SiteQuality
SIO_000300: 4.798e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.741e0

QD
type: SiteQuality
SIO_000300: 8.51e0

GenotypeQuality
all individuals: 381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34412
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2636
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4202
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.132374589514211e-4
allele num: 8831
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43519
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8773
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.662e0

QD
type: SiteQuality
SIO_000300: 3.166e1

DP
type: SiteQuality
SIO_000300: 1.201373e6

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.142726545537653e-4
allele num: 8751
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43099
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8711
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4167
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7805
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

QD
type: SiteQuality
SIO_000300: 1.917e1

FS
type: SiteQuality
SIO_000300: 1.66e0

VQSLOD
type: SiteQuality
SIO_000300: -1.38e0

DP
type: SiteQuality
SIO_000300: 1.17932e6

GenotypeQuality
all individuals: 126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8711
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4167
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.640478897422214e-5
allele num: 43099
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.28122998078155e-4
allele num: 7805
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8751
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.917e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

FS
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.17932e6

GenotypeQuality
all individuals: 1816
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31159
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 561
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7793
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.148105625717566e-4
allele num: 8710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.168256e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

FS
type: SiteQuality
SIO_000300: 8.615e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: -2.804e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.912e0

QD
type: SiteQuality
SIO_000300: 1.074e1

MQ
type: SiteQuality
SIO_000300: 5.886e1

GenotypeQuality
all individuals: 13178
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5901
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7781
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42857
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.416042522348393e-4
allele num: 4139
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 561
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.339e0

FS
type: SiteQuality
SIO_000300: 3.561e0

MQ
type: SiteQuality
SIO_000300: 5.845e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.163623e6

QD
type: SiteQuality
SIO_000300: 1.515e1

GenotypeQuality
all individuals: 124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.287664177182591e-4
allele num: 7766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5865
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8645
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42655
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.142e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.153923e6

QD
type: SiteQuality
SIO_000300: 1.275e1

MQ
type: SiteQuality
SIO_000300: 5.741e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.856e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

GenotypeQuality
all individuals: 361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2375
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27636
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5767
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4052
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7778
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42002
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 2.278e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 1.115634e6

GenotypeQuality
all individuals: 346
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.393317856544528e-5
allele num: 41783
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8467
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.105147e6

QD
type: SiteQuality
SIO_000300: 2.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
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variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 535
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7736
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.211387038158692e-4
allele num: 8255
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.063273e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e-1

QD
type: SiteQuality
SIO_000300: 2.563e1

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 476
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 533
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3849
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.668378576669112e-4
allele num: 8178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.935e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.056221e6

GenotypeQuality
all individuals: 1546
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4729
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 9.75e1
variant carriers: 42

GenotypeQuality
all individuals: 22510
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7685
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8273
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3825
num of homozygotes: 0

South Asian
type: Population
allele count: 51
allele frequency: 6.236243580337491e-3
allele num: 8178
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.99e-2

QD
type: SiteQuality
SIO_000300: 1.999e1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.404e0

DP
type: SiteQuality
SIO_000300: 1.058435e6

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7713
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 531
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5562
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.220703125e-4
allele num: 8192
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

VQSLOD
type: SiteQuality
SIO_000300: -2.205e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 2.622e0

QD
type: SiteQuality
SIO_000300: 2.191e1

DP
type: SiteQuality
SIO_000300: 1.062691e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
all individuals: 339
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7879
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5875
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3913
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42310
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 1.592e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 1.178418e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.531325148715353e-4
allele num: 7901
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.344830820456304e-5
allele num: 42647
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5929
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.348796241926013e-4
allele num: 8515
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.340823970037453e-4
allele num: 8544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3924
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.201776e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

QD
type: SiteQuality
SIO_000300: 1.653e1

FS
type: SiteQuality
SIO_000300: 5.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 557
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8553
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3961
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.658963846440551e-5
allele num: 42928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8597
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

DP
type: SiteQuality
SIO_000300: 1.212441e6

MQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.214e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

GenotypeQuality
all individuals: 38466
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 727
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variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8653
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8691
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 559
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.638806948541462e-4
allele num: 6102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43697
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.247243e6

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 1.327e0

QD
type: SiteQuality
SIO_000300: 1.078e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 561
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8715
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.247816321437484e-4
allele num: 8014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44060
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

FS
type: SiteQuality
SIO_000300: 5.389e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.893e1

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.263243e6

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
all individuals: 731
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 341
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variant carriers: 1

GenotypeQuality
all individuals: 443
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.265159580492446e-5
allele num: 44147
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8763
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8019
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8730
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.266878e6

FS
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.483e0

QD
type: SiteQuality
SIO_000300: 7.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 777
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 303
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.231678778174652e-4
allele num: 8119
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8853
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8919
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

DP
type: SiteQuality
SIO_000300: 1.313271e6

QD
type: SiteQuality
SIO_000300: 2.961e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 343
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GenotypeQuality
all individuals: 605
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.188566926376608e-5
allele num: 45692
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8926
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6335
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 587
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ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.289e-1

QD
type: SiteQuality
SIO_000300: 7.18e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45675
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9027
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East Asian
type: Population
allele count: 1
allele frequency: 1.582278481012658e-4
allele num: 6320
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4199
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8929
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.519e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.328156e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 681
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8847
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4207
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8155
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.281722e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.737e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.296e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44976
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4210
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 1.13455865668255e-4
allele num: 8814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.9e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.643e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.101e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

QD
type: SiteQuality
SIO_000300: 1.548e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8955
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.223803593666607e-5
allele num: 44968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 1.256624e6

VQSLOD
type: SiteQuality
SIO_000300: -2.774e0

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.365e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.977e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8543
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 7.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8793
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8959
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6145
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.910075067382442e-5
allele num: 44893
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.849e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

QD
type: SiteQuality
SIO_000300: 1.765e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.418e0

VQSLOD
type: SiteQuality
SIO_000300: -1.109e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.251273e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

GenotypeQuality
all individuals: 675
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34397
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6137
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44837
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8781
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.11632060727841e-4
allele num: 8958
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.142e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.882e-1

DP
type: SiteQuality
SIO_000300: 1.249018e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
all individuals: 34828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4219
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8115
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8951
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6101
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.233937985881512e-5
allele num: 44764
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

QD
type: SiteQuality
SIO_000300: 3.065e1

DP
type: SiteQuality
SIO_000300: 1.245335e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 8780
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34213
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6069
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8099
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8745
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.241599605478469e-5
allele num: 44611
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4219
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.409e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 2.921e1

DP
type: SiteQuality
SIO_000300: 1.238495e6

GenotypeQuality
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4233
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.707058060765946e-5
allele num: 44729
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.764e1

VQSLOD
type: SiteQuality
SIO_000300: -2.908e0

FS
type: SiteQuality
SIO_000300: 2.1669e1

MQRankSum
type: SiteQuality
SIO_000300: -6.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

DP
type: SiteQuality
SIO_000300: 1.236686e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.48e-1

GenotypeQuality
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.23929059274022e-5
allele num: 44657
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4233
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8753
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.858e-1

QD
type: SiteQuality
SIO_000300: 2.899e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.233009e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

GenotypeQuality
all individuals: 2983
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33107
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 460
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8739
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6055
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4231
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8939
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44575
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -9.53e-1

DP
type: SiteQuality
SIO_000300: 1.22946e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 1.633e1

GenotypeQuality
all individuals: 1038
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2890
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 8
allele frequency: 9.88875154511743e-4
allele num: 8090
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8715
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44527
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6043
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8930
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.438e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.226925e6

VQSLOD
type: SiteQuality
SIO_000300: 5.19e0

GenotypeQuality
all individuals: 401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 354
bin: 9.75e1
variant carriers: 12

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44590
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.145606598694008e-4
allele num: 8729
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.730317636880484e-3
allele num: 8091
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6053
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4237
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8936
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 2.444e0

QD
type: SiteQuality
SIO_000300: 1.658e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.227701e6

GenotypeQuality
all individuals: 391
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 466
bin: 9.75e1
variant carriers: 140

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 588
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1026
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 33953
bin: 6.25e1
variant carriers: 7

South Asian
type: Population
allele count: 9
allele frequency: 1.003009027081244e-3
allele num: 8973
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 144
allele frequency: 3.225950983467001e-3
allele num: 44638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6057
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.410151908114116e-4
allele num: 8097
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4252
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 2.853881278538813e-3
allele num: 8760
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 6.86106346483705e-3
allele num: 583
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.241917e6

QD
type: SiteQuality
SIO_000300: 2.076e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.405e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.086e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

GenotypeQuality
all individuals: 332
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8973
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8101
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44689
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 585
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.24523e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.605e0

VQSLOD
type: SiteQuality
SIO_000300: -4.057e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 1.3236e1

QD
type: SiteQuality
SIO_000300: 4.73e0

GenotypeQuality
all individuals: 227
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6229
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.672240802675585e-3
allele num: 598
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.246433786364147e-4
allele num: 8903
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8191
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.013e0

DP
type: SiteQuality
SIO_000300: 1.325493e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

FS
type: SiteQuality
SIO_000300: 3.312e0

QD
type: SiteQuality
SIO_000300: 1.719e1

VQSLOD
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 335
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3197
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.185983473964937e-5
allele num: 45746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6241
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4341
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

QD
type: SiteQuality
SIO_000300: 2.256e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.68e0

VQSLOD
type: SiteQuality
SIO_000300: -2.291e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 1.331018e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 592
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.169479758753851e-5
allele num: 46094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8231
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6293
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.350635e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.01e0

QD
type: SiteQuality
SIO_000300: 1.054e1

FS
type: SiteQuality
SIO_000300: 1.366e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

GenotypeQuality
all individuals: 47
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6387
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8279
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46484
num of homozygotes: 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: 613
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9383
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4407
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.541e1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.382029e6

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3496
bin: 6.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9034
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.062699256110521e-4
allele num: 9410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6395
num of homozygotes: 0

African
type: Population
allele count: 83
allele frequency: 1.001206272617612e-2
allele num: 8290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46535
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.386728e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: 8.140000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.237e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.675e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

GenotypeQuality
all individuals: 330
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2867
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.099384344766931e-4
allele num: 9096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8349
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46922
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9541
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.405512e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.825e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.394e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.504e0

GenotypeQuality
all individuals: 2796
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48924
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8355
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.390456917669613e-5
allele num: 46945
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4443
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 8.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.79e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

DP
type: SiteQuality
SIO_000300: 1.407088e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

QD
type: SiteQuality
SIO_000300: 1.538e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
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variant carriers: 0

GenotypeQuality
all individuals: 460
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9635
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8377
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.121700755325469e-5
allele num: 47132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6487
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9115
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.342e1

VQSLOD
type: SiteQuality
SIO_000300: 2.13e-1

DP
type: SiteQuality
SIO_000300: 1.418367e6

GenotypeQuality
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
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variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4487
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9173
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6515
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8453
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47551
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9857
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

DP
type: SiteQuality
SIO_000300: 1.442379e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

FS
type: SiteQuality
SIO_000300: 7.653e0

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-2

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.75e1
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GenotypeQuality
all individuals: 50300
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8465
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9175
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9879
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.10176758654028e-5
allele num: 47579
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6519
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.446468e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.52e1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3927
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4499
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9915
num of homozygotes: 0

East Asian
type: Population
allele count: 92
allele frequency: 1.411692496547491e-2
allele num: 6517
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8469
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 1.119e1

QD
type: SiteQuality
SIO_000300: 2.019e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.455689e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.684e-1

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6587
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10061
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.791e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

VQSLOD
type: SiteQuality
SIO_000300: -2.622e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.316e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.17e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.477662e6

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

GenotypeQuality
all individuals: 348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4153
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
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: 6587
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.939369843951894e-5
allele num: 10061
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 2.791e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.316e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -2.622e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 1.477662e6

GenotypeQuality
all individuals: 4160
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.517680983457277e-4
allele num: 6589
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47861
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.305e0

VQSLOD
type: SiteQuality
SIO_000300: 8.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.77e-1

QD
type: SiteQuality
SIO_000300: 1.697e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

FS
type: SiteQuality
SIO_000300: 3.906e0

DP
type: SiteQuality
SIO_000300: 1.478494e6

GenotypeQuality
all individuals: 332
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4195
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.922603691208574e-5
allele num: 10078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6605
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47885
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

DP
type: SiteQuality
SIO_000300: 1.480714e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.477e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.72e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 2.905e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10083
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47891
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9229
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.21483942414175e-4
allele num: 4515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.05e1

FS
type: SiteQuality
SIO_000300: 4.989e0

MQ
type: SiteQuality
SIO_000300: 5.019e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 5.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.553e-1

DP
type: SiteQuality
SIO_000300: 1.48184e6

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47909
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.08283703302653e-4
allele num: 9235
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

DP
type: SiteQuality
SIO_000300: 1.484076e6

FS
type: SiteQuality
SIO_000300: 1.856e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.203e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
SIO_000300: 5.917e1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.124e0

QD
type: SiteQuality
SIO_000300: 1.089e1

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.04331858776396e-4
allele num: 47924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.906875371507826e-5
allele num: 10094
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.88e-1

DP
type: SiteQuality
SIO_000300: 1.485544e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.396e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 1.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.066e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 2.123e1

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
bin: 9.75e1
variant carriers: 13

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 1.287638668779715e-3
allele num: 10096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47924
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.510117789187557e-4
allele num: 6622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.68e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

QD
type: SiteQuality
SIO_000300: 1.342e1

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 1.836e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.32e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.486554e6

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 53777
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GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e0

MQ
type: SiteQuality
SIO_000300: 5.709e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.598e0

VQSLOD
type: SiteQuality
SIO_000300: -2.115e1

FS
type: SiteQuality
SIO_000300: 5.7939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.858e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.937e0

DP
type: SiteQuality
SIO_000300: 1.486793e6

QD
type: SiteQuality
SIO_000300: 1.05e0

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

GenotypeQuality
all individuals: 57
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086506562063138e-5
allele num: 47927
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10101
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9247
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.35e-2

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

DP
type: SiteQuality
SIO_000300: 1.486911e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 3.016e1

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 874
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
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GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47935
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.176055509820064e-4
allele num: 8503
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.488159e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.332e1

MQRankSum
type: SiteQuality
SIO_000300: -1.033e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.341e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47930
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.968533544429052e-4
allele num: 10106
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
type: SiteQuality
SIO_000300: 1.807e1

FS
type: SiteQuality
SIO_000300: 4.696e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.48835e6

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 70
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GenotypeQuality
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GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 565
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8497
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.172838991007532e-5
allele num: 47929
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.177e1

DP
type: SiteQuality
SIO_000300: 1.488601e6

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 6.851e0

VQSLOD
type: SiteQuality
SIO_000300: -6.108e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.71e-2

QD
type: SiteQuality
SIO_000300: 2.288e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47933
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.176470588235294e-4
allele num: 8500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.836e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

DP
type: SiteQuality
SIO_000300: 1.488763e6

QD
type: SiteQuality
SIO_000300: 1.407e1

FS
type: SiteQuality
SIO_000300: 5.191e0

GenotypeQuality
all individuals: 53734
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4279
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.177301624676242e-4
allele num: 8494
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.607e0

FS
type: SiteQuality
SIO_000300: 3.445e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.399e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.48937e6

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9255
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47927
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.489213e6

MQRankSum
type: SiteQuality
SIO_000300: -1.299e0

MQ
type: SiteQuality
SIO_000300: 4.015e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.347e1

FS
type: SiteQuality
SIO_000300: 4.7523e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4287
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47933
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: 8495
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.080146899978397e-4
allele num: 9258
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

DP
type: SiteQuality
SIO_000300: 1.48925e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.198e1

GenotypeQuality
all individuals: 4291
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08620186089206e-5
allele num: 47934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

VQSLOD
type: SiteQuality
SIO_000300: 9.44e-1

DP
type: SiteQuality
SIO_000300: 1.489282e6

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.03e-2

MQ
type: SiteQuality
SIO_000300: 5.871e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeQuality
all individuals: 53789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
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variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.75e1
variant carriers: 3

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9257
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.354880489815142e-4
allele num: 8493
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08620186089206e-5
allele num: 47934
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.669e0

DP
type: SiteQuality
SIO_000300: 1.489517e6

QD
type: SiteQuality
SIO_000300: 1.983e1

MQRankSum
type: SiteQuality
SIO_000300: -6.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.797e0

VQSLOD
type: SiteQuality
SIO_000300: -3.555e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.32e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 4310
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47937
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.565e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-2

DP
type: SiteQuality
SIO_000300: 1.489725e6

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
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: 1
allele frequency: 1.177024482109228e-4
allele num: 8496
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9265
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47937
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-2

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.119e0

DP
type: SiteQuality
SIO_000300: 1.48967e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

QD
type: SiteQuality
SIO_000300: 1.21e1

MQ
type: SiteQuality
SIO_000300: 5.88e1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508068164681044e-4
allele num: 6631
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47929
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.212e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.718e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 53722
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GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08620186089206e-5
allele num: 47934
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.87e-1

DP
type: SiteQuality
SIO_000300: 1.489768e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.003e0

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.403e1

FS
type: SiteQuality
SIO_000300: 3.037e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.86e0

VQSLOD
type: SiteQuality
SIO_000300: -8.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.17e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 48
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.893153937475267e-5
allele num: 10108
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47937
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.68e-2

QD
type: SiteQuality
SIO_000300: 3.259e1

DP
type: SiteQuality
SIO_000300: 1.489722e6

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

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6627
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086332436210386e-5
allele num: 47931
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.563e-1

DP
type: SiteQuality
SIO_000300: 1.489849e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.791e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 4.517e1

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47927
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.509889778046203e-4
allele num: 6623
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.489836e6

QD
type: SiteQuality
SIO_000300: 3.352e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.29e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0