12-123380655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123380655
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123380655
    reference: chr 12
allele count: 1
allele frequency: 1.392408588376173e-5
allele num: 71818
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000267202
  ensembl transcript: ENST00000267202
  gene symbol: VPS37B
  hgvsc: ENST00000267202.2:c.-46G>A
  variant of: http://identifiers.org/hgnc/25754
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000446075
  ensembl transcript: ENST00000535765
  gene symbol: VPS37B
  hgvsc: ENST00000535765.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/25754
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  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
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  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
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4276
  num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

12-123380656-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123380656
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123380655
    reference: chr 12
allele count: 1
allele frequency: 1.392602495543672e-5
allele num: 71808
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000267202
  ensembl transcript: ENST00000267202
  gene symbol: VPS37B
  hgvsc: ENST00000267202.2:c.-48delG
  variant of: http://identifiers.org/hgnc/25754
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000446075
  ensembl transcript: ENST00000535765
  gene symbol: VPS37B
  hgvsc: ENST00000535765.1:c.-48delG
  variant of: http://identifiers.org/hgnc/25754
canonical: true
consequence: 5' UTR
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  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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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  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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  bin: 4.75e1
  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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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4508
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5018
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: TC
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

12-123380657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123380657
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123380657
    reference: chr 12
allele count: 1
allele frequency: 1.44275161588181e-5
allele num: 69312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000267202
  ensembl transcript: ENST00000267202
  gene symbol: VPS37B
  hgvsc: ENST00000267202.2:c.-48G>A
  variant of: http://identifiers.org/hgnc/25754
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000446075
  ensembl transcript: ENST00000535765
  gene symbol: VPS37B
  hgvsc: ENST00000535765.1:c.-48G>A
  variant of: http://identifiers.org/hgnc/25754
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  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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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: 7.5e0
  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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  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: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9402
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

12-123380659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123380659
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123380659
    reference: chr 12
allele count: 1
allele frequency: 1.544115376300917e-5
allele num: 64762
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000267202
  ensembl transcript: ENST00000267202
  gene symbol: VPS37B
  hgvsc: ENST00000267202.2:c.-50C>T
  variant of: http://identifiers.org/hgnc/25754
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000446075
  ensembl transcript: ENST00000535765
  gene symbol: VPS37B
  hgvsc: ENST00000535765.1:c.-50C>T
  variant of: http://identifiers.org/hgnc/25754
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 68
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6630
  num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

12-123380660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123380660
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123380660
    reference: chr 12
allele count: 1
allele frequency: 1.621323648626739e-5
allele num: 61678
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000267202
  ensembl transcript: ENST00000267202
  gene symbol: VPS37B
  hgvsc: ENST00000267202.2:c.-51G>A
  variant of: http://identifiers.org/hgnc/25754
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000446075
  ensembl transcript: ENST00000535765
  gene symbol: VPS37B
  hgvsc: ENST00000535765.1:c.-51G>A
  variant of: http://identifiers.org/hgnc/25754
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12022
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3801
  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3738
  num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

12-123380661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123380661
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123380661
    reference: chr 12
allele count: 1
allele frequency: 1.988229680292667e-5
allele num: 50296
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000267202
  ensembl transcript: ENST00000267202
  gene symbol: VPS37B
  hgvsc: ENST00000267202.2:c.-52G>A
  variant of: http://identifiers.org/hgnc/25754
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000139722
  ensembl protein: ENSP00000446075
  ensembl transcript: ENST00000535765
  gene symbol: VPS37B
  hgvsc: ENST00000535765.1:c.-52G>A
  variant of: http://identifiers.org/hgnc/25754
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 246
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3676
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-123405574-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123405574
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123405574
    reference: chr 12
allele count: 1
allele frequency: 9.293680297397769e-5
allele num: 10760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.*11T>G
  variant of: http://identifiers.org/hgnc/50
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  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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  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
  all individuals: 84
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
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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: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 92
  num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

12-123409300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123409300
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123409300
    reference: chr 12
allele count: 2
allele frequency: 1.853224610822832e-4
allele num: 10792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2041-3710T>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.*46T>C
  variant of: http://identifiers.org/hgnc/50
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 4994
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 1
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4
  num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

12-123409310-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123409310
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123409310
    reference: chr 12
allele count: 46
allele frequency: 4.265578635014837e-3
allele num: 10784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.*36A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2041-3720A>G
  variant of: http://identifiers.org/hgnc/50
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 399
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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
  all individuals: 2761
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
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genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4996
  bin: 9.75e1
  variant carriers: 42
num of homozygotes: 2
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.08695652173913e-2
  allele num: 92
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

12-123414415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414415
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414415
    reference: chr 12
allele count: 1
allele frequency: 1.594184415253157e-5
allele num: 62728
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*43C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*43C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2324C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*43C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*43C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2324C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3684
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6449
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3034
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

12-123414419-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414419
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414419
    reference: chr 12
allele count: 2
allele frequency: 3.193867773874162e-5
allele num: 62620
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2320G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*39G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2320G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*39G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*39G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*39G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19746
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9053
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5336
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6615
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

12-123414419-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414419
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414419
    reference: chr 12
allele count: 1
allele frequency: 1.596933886937081e-5
allele num: 62620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*39G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2320G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*39G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*39G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*39G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*39G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*39G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2320G>C
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6615
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3608
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

12-123414433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414433
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414433
    reference: chr 12
allele count: 2
allele frequency: 3.107809926344905e-5
allele num: 64354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*25G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*25G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2306G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*25G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*25G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*25G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*25G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2306G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-123414436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414436
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414436
    reference: chr 12
allele count: 2
allele frequency: 3.100102303376012e-5
allele num: 64514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2303G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*22G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2303G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*22G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*22G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*22G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11198
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21097
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14782
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15621
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

12-123414437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414437
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414437
    reference: chr 12
allele count: 57
allele frequency: 8.78626260135031e-4
allele num: 64874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*21C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*21C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2302C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2302C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*21C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*21C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21166
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22317
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5715
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

12-123414439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414439
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414439
    reference: chr 12
allele count: 33
allele frequency: 5.019622159350187e-4
allele num: 65742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*19C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*19C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*19C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2300C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2300C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*19C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*19C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*19C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15903
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21312
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3286
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16943
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22981
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/12-123414446-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414446
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414446
    reference: chr 12
allele count: 1
allele frequency: 1.492091912861832e-5
allele num: 67020
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*12T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*12T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*12T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*12T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*12T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2293T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2293T>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*12T>G
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18468
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-123414450-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414450
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414451
    reference: chr 12
allele count: 4
allele frequency: 5.936655881741815e-5
allele num: 67378
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*7dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*7dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*7dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2288dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*7dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*7dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*7dupG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2288dupG
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18745
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24012
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20135
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

12-123414454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414454
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414454
    reference: chr 12
allele count: 1
allele frequency: 1.467911455580999e-5
allele num: 68124
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2285G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.*4G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.*4G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.*4G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2285G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.*4G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24650
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/12-123414459-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414459
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414459
    reference: chr 12
allele count: 1
allele frequency: 1.460323023452788e-5
allele num: 68478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2171G>T
  hgvsp: ENSP00000280559.7:p.Ter724LeuextTer79
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2111G>T
  hgvsp: ENSP00000441734.1:p.Ter704LeuextTer79
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2300G>T
  hgvsp: ENSP00000440288.1:p.Ter767LeuextTer79
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2309G>T
  hgvsp: ENSP00000394898.2:p.Ter770LeuextTer79
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2300G>T
  hgvsp: ENSP00000376234.3:p.Ter767LeuextTer79
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2300G>T
  hgvsp: ENSP00000280560.8:p.Ter767LeuextTer79
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2280G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2280G>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25436
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ter767LeuextTer79
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

12-123414462-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414462
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414461
    reference: chr 12
allele count: 3
allele frequency: 4.39161494320178e-5
allele num: 68312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2296delG
  hgvsp: ENSP00000280560.8:p.Ala766ProfsTer78
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2296delG
  hgvsp: ENSP00000440288.1:p.Ala766ProfsTer78
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2276delG
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2107delG
  hgvsp: ENSP00000441734.1:p.Ala703ProfsTer78
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2167delG
  hgvsp: ENSP00000280559.7:p.Ala723ProfsTer78
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2296delG
  hgvsp: ENSP00000376234.3:p.Ala766ProfsTer78
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2305delG
  hgvsp: ENSP00000394898.2:p.Ala769ProfsTer78
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2276delG
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala766ProfsTer78
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: GC
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-123414463-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414463
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414463
    reference: chr 12
allele count: 1
allele frequency: 1.463186234343907e-5
allele num: 68344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2296G>T
  hgvsp: ENSP00000376234.3:p.Ala766Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2276G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2296G>T
  hgvsp: ENSP00000280560.8:p.Ala766Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2167G>T
  hgvsp: ENSP00000280559.7:p.Ala723Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2107G>T
  hgvsp: ENSP00000441734.1:p.Ala703Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2276G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2296G>T
  hgvsp: ENSP00000440288.1:p.Ala766Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2305G>T
  hgvsp: ENSP00000394898.2:p.Ala769Ser
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22592
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala766Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

12-123414463-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414463
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414463
    reference: chr 12
allele count: 4
allele frequency: 5.852744937375629e-5
allele num: 68344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2296G>C
  hgvsp: ENSP00000376234.3:p.Ala766Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2276G>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2296G>C
  hgvsp: ENSP00000280560.8:p.Ala766Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2107G>C
  hgvsp: ENSP00000441734.1:p.Ala703Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2296G>C
  hgvsp: ENSP00000440288.1:p.Ala766Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2167G>C
  hgvsp: ENSP00000280559.7:p.Ala723Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2305G>C
  hgvsp: ENSP00000394898.2:p.Ala769Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2276G>C
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22592
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Ala766Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

12-123414463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414463
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414463
    reference: chr 12
allele count: 2
allele frequency: 2.926372468687814e-5
allele num: 68344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2167G>A
  hgvsp: ENSP00000280559.7:p.Ala723Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2305G>A
  hgvsp: ENSP00000394898.2:p.Ala769Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2276G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2107G>A
  hgvsp: ENSP00000441734.1:p.Ala703Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2276G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2296G>A
  hgvsp: ENSP00000280560.8:p.Ala766Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2296G>A
  hgvsp: ENSP00000376234.3:p.Ala766Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2296G>A
  hgvsp: ENSP00000440288.1:p.Ala766Thr
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 20725
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala766Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

12-123414464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414464
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414464
    reference: chr 12
allele count: 32
allele frequency: 4.697868342239709e-4
allele num: 68116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2304G>A
  hgvsp: ENST00000442028.2:c.2304G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2166G>A
  hgvsp: ENST00000346530.5:c.2166G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2295G>A
  hgvsp: ENST00000280560.8:c.2295G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2295G>A
  hgvsp: ENST00000542678.1:c.2295G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2275G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2295G>A
  hgvsp: ENST00000392439.3:c.2295G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2275G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2106G>A
  hgvsp: ENST00000540285.1:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8450
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22714
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18264
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26399
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys765Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

12-123414465-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414465
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414465
    reference: chr 12
allele count: 1
allele frequency: 1.465545036198962e-5
allele num: 68234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2294A>G
  hgvsp: ENSP00000280560.8:p.Lys765Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2165A>G
  hgvsp: ENSP00000280559.7:p.Lys722Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2274A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2105A>G
  hgvsp: ENSP00000441734.1:p.Lys702Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2294A>G
  hgvsp: ENSP00000376234.3:p.Lys765Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2274A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2294A>G
  hgvsp: ENSP00000440288.1:p.Lys765Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2303A>G
  hgvsp: ENSP00000394898.2:p.Lys768Arg
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18349
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3451
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1978
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Lys765Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

12-123414468-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414468
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414468
    reference: chr 12
allele count: 2
allele frequency: 2.964631940944532e-5
allele num: 67462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2271A>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2162A>C
  hgvsp: ENSP00000280559.7:p.His721Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2271A>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2291A>C
  hgvsp: ENSP00000280560.8:p.His764Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2102A>C
  hgvsp: ENSP00000441734.1:p.His701Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2300A>C
  hgvsp: ENSP00000394898.2:p.His767Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2291A>C
  hgvsp: ENSP00000376234.3:p.His764Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2291A>C
  hgvsp: ENSP00000440288.1:p.His764Pro
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17235
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27352
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His764Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

12-123414469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414469
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414469
    reference: chr 12
allele count: 1
allele frequency: 1.47920241405834e-5
allele num: 67604
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2290C>T
  hgvsp: ENSP00000440288.1:p.His764Tyr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2161C>T
  hgvsp: ENSP00000280559.7:p.His721Tyr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2101C>T
  hgvsp: ENSP00000441734.1:p.His701Tyr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2270C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2290C>T
  hgvsp: ENSP00000280560.8:p.His764Tyr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2270C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2290C>T
  hgvsp: ENSP00000376234.3:p.His764Tyr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2299C>T
  hgvsp: ENSP00000394898.2:p.His767Tyr
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His764Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

12-123414473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414473
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414473
    reference: chr 12
allele count: 1
allele frequency: 1.487033071615513e-5
allele num: 67248
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2286C>T
  hgvsp: ENST00000542678.1:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2097C>T
  hgvsp: ENST00000540285.1:c.2097C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2295C>T
  hgvsp: ENST00000442028.2:c.2295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2286C>T
  hgvsp: ENST00000280560.8:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2266C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2266C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2157C>T
  hgvsp: ENST00000346530.5:c.2157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2286C>T
  hgvsp: ENST00000392439.3:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3391
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly762Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

12-123414475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414475
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414475
    reference: chr 12
allele count: 4
allele frequency: 5.984619527813519e-5
allele num: 66838
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2284G>A
  hgvsp: ENSP00000440288.1:p.Gly762Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2284G>A
  hgvsp: ENSP00000280560.8:p.Gly762Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2264G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2264G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2095G>A
  hgvsp: ENSP00000441734.1:p.Gly699Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2293G>A
  hgvsp: ENSP00000394898.2:p.Gly765Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2284G>A
  hgvsp: ENSP00000376234.3:p.Gly762Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2155G>A
  hgvsp: ENSP00000280559.7:p.Gly719Ser
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9795
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly762Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

12-123414476-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414476
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414476
    reference: chr 12
allele count: 8
allele frequency: 1.202501202501203e-4
allele num: 66528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2263C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2094C>T
  hgvsp: ENST00000540285.1:c.2094C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2283C>T
  hgvsp: ENST00000392439.3:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2292C>T
  hgvsp: ENST00000442028.2:c.2292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2263C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2283C>T
  hgvsp: ENST00000280560.8:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2154C>T
  hgvsp: ENST00000346530.5:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2283C>T
  hgvsp: ENST00000542678.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10037
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15636
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn761Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

12-123414481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414481
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414481
    reference: chr 12
allele count: 3
allele frequency: 4.79447676276929e-5
allele num: 62572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2278G>A
  hgvsp: ENSP00000280560.8:p.Ala760Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2089G>A
  hgvsp: ENSP00000441734.1:p.Ala697Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2258G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2149G>A
  hgvsp: ENSP00000280559.7:p.Ala717Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2258G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2278G>A
  hgvsp: ENSP00000440288.1:p.Ala760Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2287G>A
  hgvsp: ENSP00000394898.2:p.Ala763Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2278G>A
  hgvsp: ENSP00000376234.3:p.Ala760Thr
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30425
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala760Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-123414485-AGGCTCGTTGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414485
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414475
    reference: chr 12
allele count: 21
allele frequency: 3.428123673642626e-4
allele num: 61258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsp: ENSP00000280560.8:p.His755LeufsTer2
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsp: ENSP00000280559.7:p.His712LeufsTer2
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsp: ENSP00000440288.1:p.His755LeufsTer2
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsp: ENSP00000441734.1:p.His692LeufsTer2
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsp: ENSP00000394898.2:p.His758LeufsTer2
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsp: ENSP00000376234.3:p.His755LeufsTer2
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12744
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24908
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4590
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31124
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His755LeufsTer2
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: AGGCTCGTTGT
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

12-123414490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414490
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414490
    reference: chr 12
allele count: 7
allele frequency: 1.181354845242515e-4
allele num: 59254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2140G>A
  hgvsp: ENSP00000280559.7:p.Glu714Lys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2269G>A
  hgvsp: ENSP00000280560.8:p.Glu757Lys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2278G>A
  hgvsp: ENSP00000394898.2:p.Glu760Lys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2269G>A
  hgvsp: ENSP00000376234.3:p.Glu757Lys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2249G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2269G>A
  hgvsp: ENSP00000440288.1:p.Glu757Lys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2080G>A
  hgvsp: ENSP00000441734.1:p.Glu694Lys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2249G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9305
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25481
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13135
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu757Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

12-123414494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414494
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414494
    reference: chr 12
allele count: 2
allele frequency: 3.526217426566522e-5
allele num: 56718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2245C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2265C>T
  hgvsp: ENST00000542678.1:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2265C>T
  hgvsp: ENST00000280560.8:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2076C>T
  hgvsp: ENST00000540285.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2274C>T
  hgvsp: ENST00000442028.2:c.2274C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2136C>T
  hgvsp: ENST00000346530.5:c.2136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2265C>T
  hgvsp: ENST00000392439.3:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2245C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5579
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His755His
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

12-123414497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414497
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414497
    reference: chr 12
allele count: 1
allele frequency: 1.751313485113835e-5
allele num: 57100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2262C>T
  hgvsp: ENST00000280560.8:c.2262C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2262C>T
  hgvsp: ENST00000392439.3:c.2262C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2073C>T
  hgvsp: ENST00000540285.1:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2262C>T
  hgvsp: ENST00000542678.1:c.2262C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2133C>T
  hgvsp: ENST00000346530.5:c.2133C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2242C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2271C>T
  hgvsp: ENST00000442028.2:c.2271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2242C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8627
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32958
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10238
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly754Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

12-123414499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414499
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414499
    reference: chr 12
allele count: 1
allele frequency: 1.766472354707649e-5
allele num: 56610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2260G>A
  hgvsp: ENSP00000280560.8:p.Gly754Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2131G>A
  hgvsp: ENSP00000280559.7:p.Gly711Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2071G>A
  hgvsp: ENSP00000441734.1:p.Gly691Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2240G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2260G>A
  hgvsp: ENSP00000440288.1:p.Gly754Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2269G>A
  hgvsp: ENSP00000394898.2:p.Gly757Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2240G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2260G>A
  hgvsp: ENSP00000376234.3:p.Gly754Ser
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly754Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

12-123414500-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414500
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414500
    reference: chr 12
allele count: 1
allele frequency: 1.777272242562116e-5
allele num: 56266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2070T>C
  hgvsp: ENST00000540285.1:c.2070T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2130T>C
  hgvsp: ENST00000346530.5:c.2130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2268T>C
  hgvsp: ENST00000442028.2:c.2268T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2239T>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2239T>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2259T>C
  hgvsp: ENST00000280560.8:c.2259T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2259T>C
  hgvsp: ENST00000542678.1:c.2259T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2259T>C
  hgvsp: ENST00000392439.3:c.2259T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6039
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala753Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

12-123414505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414505
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414505
    reference: chr 12
allele count: 1
allele frequency: 1.845154623957488e-5
allele num: 54196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2263A>G
  hgvsp: ENSP00000394898.2:p.Thr755Ala
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2234A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2125A>G
  hgvsp: ENSP00000280559.7:p.Thr709Ala
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2065A>G
  hgvsp: ENSP00000441734.1:p.Thr689Ala
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2254A>G
  hgvsp: ENSP00000280560.8:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2254A>G
  hgvsp: ENSP00000440288.1:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2254A>G
  hgvsp: ENSP00000376234.3:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2234A>G
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14557
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr752Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

12-123414514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414514
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414514
    reference: chr 12
allele count: 20
allele frequency: 4.32264199878966e-4
allele num: 46268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2254G>A
  hgvsp: ENSP00000394898.2:p.Ala752Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2116G>A
  hgvsp: ENSP00000280559.7:p.Ala706Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2245G>A
  hgvsp: ENSP00000280560.8:p.Ala749Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2245G>A
  hgvsp: ENSP00000376234.3:p.Ala749Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2225G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2056G>A
  hgvsp: ENSP00000441734.1:p.Ala686Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2245G>A
  hgvsp: ENSP00000440288.1:p.Ala749Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2225G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14055
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26998
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9416
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala749Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

12-123414515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414515
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414515
    reference: chr 12
allele count: 3
allele frequency: 6.451890403888339e-5
allele num: 46498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2055C>T
  hgvsp: ENST00000540285.1:c.2055C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2244C>T
  hgvsp: ENST00000542678.1:c.2244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2244C>T
  hgvsp: ENST00000280560.8:c.2244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2244C>T
  hgvsp: ENST00000392439.3:c.2244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2224C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2224C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2115C>T
  hgvsp: ENST00000346530.5:c.2115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2253C>T
  hgvsp: ENST00000442028.2:c.2253C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27162
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13846
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30991
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala748Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

12-123414517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414517
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414517
    reference: chr 12
allele count: 4
allele frequency: 9.03954802259887e-5
allele num: 44250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2242G>A
  hgvsp: ENSP00000280560.8:p.Ala748Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2251G>A
  hgvsp: ENSP00000394898.2:p.Ala751Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2222G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2242G>A
  hgvsp: ENSP00000440288.1:p.Ala748Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2222G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2242G>A
  hgvsp: ENSP00000376234.3:p.Ala748Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2053G>A
  hgvsp: ENSP00000441734.1:p.Ala685Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2113G>A
  hgvsp: ENSP00000280559.7:p.Ala705Thr
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13232
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9935
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala748Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

12-123414518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414518
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414518
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 44990
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2241C>T
  hgvsp: ENST00000542678.1:c.2241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2241C>T
  hgvsp: ENST00000392439.3:c.2241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2052C>T
  hgvsp: ENST00000540285.1:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2221C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2241C>T
  hgvsp: ENST00000280560.8:c.2241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2250C>T
  hgvsp: ENST00000442028.2:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2221C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2112C>T
  hgvsp: ENST00000346530.5:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 27522
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro747Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

12-123414527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414527
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414527
    reference: chr 12
allele count: 1
allele frequency: 2.369331374686064e-5
allele num: 42206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2212G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2212G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2103G>A
  hgvsp: ENST00000346530.5:c.2103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2043G>A
  hgvsp: ENST00000540285.1:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2241G>A
  hgvsp: ENST00000442028.2:c.2241G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2232G>A
  hgvsp: ENST00000280560.8:c.2232G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2232G>A
  hgvsp: ENST00000392439.3:c.2232G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2232G>A
  hgvsp: ENST00000542678.1:c.2232G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly744Gly
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum

12-123414533-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414533
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414533
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 39732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2226G>A
  hgvsp: ENSP00000376234.3:p.Met742Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2235G>A
  hgvsp: ENSP00000394898.2:p.Met745Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2226G>A
  hgvsp: ENSP00000280560.8:p.Met742Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2226G>A
  hgvsp: ENSP00000440288.1:p.Met742Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2037G>A
  hgvsp: ENSP00000441734.1:p.Met679Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2206G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2206G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2097G>A
  hgvsp: ENSP00000280559.7:p.Met699Ile
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11884
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27799
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12243
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3419
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met742Ile
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

12-123414534-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414534
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414534
    reference: chr 12
allele count: 8
allele frequency: 2.017959842599132e-4
allele num: 39644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2225T>C
  hgvsp: ENSP00000376234.3:p.Met742Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2036T>C
  hgvsp: ENSP00000441734.1:p.Met679Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2096T>C
  hgvsp: ENSP00000280559.7:p.Met699Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2205T>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2234T>C
  hgvsp: ENSP00000394898.2:p.Met745Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2225T>C
  hgvsp: ENSP00000440288.1:p.Met742Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2225T>C
  hgvsp: ENSP00000280560.8:p.Met742Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2205T>C
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27843
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10610
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6547
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met742Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

12-123414540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414540
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414540
    reference: chr 12
allele count: 2
allele frequency: 5.217572785140353e-5
allele num: 38332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2199G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2199G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2219G>A
  hgvsp: ENSP00000376234.3:p.Arg740Gln
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2219G>A
  hgvsp: ENSP00000280560.8:p.Arg740Gln
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2090G>A
  hgvsp: ENSP00000280559.7:p.Arg697Gln
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2219G>A
  hgvsp: ENSP00000440288.1:p.Arg740Gln
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2030G>A
  hgvsp: ENSP00000441734.1:p.Arg677Gln
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2228G>A
  hgvsp: ENSP00000394898.2:p.Arg743Gln
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27919
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10001
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12889
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg740Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

12-123414541-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414541
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414541
    reference: chr 12
allele count: 2
allele frequency: 5.341024408481547e-5
allele num: 37446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2089C>T
  hgvsp: ENSP00000280559.7:p.Arg697Trp
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2029C>T
  hgvsp: ENSP00000441734.1:p.Arg677Trp
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2227C>T
  hgvsp: ENSP00000394898.2:p.Arg743Trp
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2218C>T
  hgvsp: ENSP00000440288.1:p.Arg740Trp
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2218C>T
  hgvsp: ENSP00000376234.3:p.Arg740Trp
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2218C>T
  hgvsp: ENSP00000280560.8:p.Arg740Trp
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2198C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2198C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9785
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6733
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg740Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

12-123414547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414547
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414547
    reference: chr 12
allele count: 1
allele frequency: 2.738075680411807e-5
allele num: 36522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2192G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2212G>A
  hgvsp: ENSP00000280560.8:p.Val738Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2083G>A
  hgvsp: ENSP00000280559.7:p.Val695Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2212G>A
  hgvsp: ENSP00000440288.1:p.Val738Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2221G>A
  hgvsp: ENSP00000394898.2:p.Val741Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2212G>A
  hgvsp: ENSP00000376234.3:p.Val738Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2023G>A
  hgvsp: ENSP00000441734.1:p.Val675Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2192G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6986
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13834
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val738Met
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

12-123414556-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414556
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414556
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 32982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2183G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2203G>A
  hgvsp: ENSP00000376234.3:p.Ala735Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2203G>A
  hgvsp: ENSP00000280560.8:p.Ala735Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2014G>A
  hgvsp: ENSP00000441734.1:p.Ala672Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2203G>A
  hgvsp: ENSP00000440288.1:p.Ala735Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2212G>A
  hgvsp: ENSP00000394898.2:p.Ala738Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2074G>A
  hgvsp: ENSP00000280559.7:p.Ala692Thr
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2183G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27481
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4689
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala735Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

12-123414557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414557
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414557
    reference: chr 12
allele count: 4
allele frequency: 1.211020284589767e-4
allele num: 33030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2182C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2202C>T
  hgvsp: ENST00000542678.1:c.2202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2202C>T
  hgvsp: ENST00000392439.3:c.2202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2073C>T
  hgvsp: ENST00000346530.5:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2211C>T
  hgvsp: ENST00000442028.2:c.2211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2182C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2202C>T
  hgvsp: ENST00000280560.8:c.2202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2013C>T
  hgvsp: ENST00000540285.1:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6833
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr734Tyr
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

12-123414561-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414561
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414561
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 32568
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2009T>C
  hgvsp: ENSP00000441734.1:p.Leu670Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2198T>C
  hgvsp: ENSP00000280560.8:p.Leu733Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.830T>C
  hgvsp: ENSP00000442281.1:p.Leu277Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2178T>C
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2198T>C
  hgvsp: ENSP00000376234.3:p.Leu733Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2069T>C
  hgvsp: ENSP00000280559.7:p.Leu690Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2207T>C
  hgvsp: ENSP00000394898.2:p.Leu736Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2198T>C
  hgvsp: ENSP00000440288.1:p.Leu733Pro
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2178T>C
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27694
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15655
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu733Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

12-123414565-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414565
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414565
    reference: chr 12
allele count: 3
allele frequency: 9.635767970707265e-5
allele num: 31134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.2005G>A
  hgvsp: ENSP00000441734.1:p.Gly669Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2194G>A
  hgvsp: ENSP00000280560.8:p.Gly732Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2194G>A
  hgvsp: ENSP00000376234.3:p.Gly732Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2203G>A
  hgvsp: ENSP00000394898.2:p.Gly735Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.826G>A
  hgvsp: ENSP00000442281.1:p.Gly276Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2174G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2194G>A
  hgvsp: ENSP00000440288.1:p.Gly732Ser
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2174G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2065G>A
  hgvsp: ENSP00000280559.7:p.Gly689Ser
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27887
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly732Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/12-123414578-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414578
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414578
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 29550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2181G>T
  hgvsp: ENST00000280560.8:c.2181G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2190G>T
  hgvsp: ENST00000442028.2:c.2190G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2161G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.813G>T
  hgvsp: ENST00000546289.1:c.813G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2181G>T
  hgvsp: ENST00000392439.3:c.2181G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2052G>T
  hgvsp: ENST00000346530.5:c.2052G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2181G>T
  hgvsp: ENST00000542678.1:c.2181G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1992G>T
  hgvsp: ENST00000540285.1:c.1992G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2161G>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27648
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu727Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

12-123414582-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414582
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414582
    reference: chr 12
allele count: 1
allele frequency: 3.498950314905528e-5
allele num: 28580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2177A>G
  hgvsp: ENSP00000280560.8:p.Gln726Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.809A>G
  hgvsp: ENSP00000442281.1:p.Gln270Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2048A>G
  hgvsp: ENSP00000280559.7:p.Gln683Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2186A>G
  hgvsp: ENSP00000394898.2:p.Gln729Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2177A>G
  hgvsp: ENSP00000440288.1:p.Gln726Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2157A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2157A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1988A>G
  hgvsp: ENSP00000441734.1:p.Gln663Arg
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2177A>G
  hgvsp: ENSP00000376234.3:p.Gln726Arg
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18007
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6943
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln726Arg
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

12-123414587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414587
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414587
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 28474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2172C>T
  hgvsp: ENST00000280560.8:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2172C>T
  hgvsp: ENST00000392439.3:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2043C>T
  hgvsp: ENST00000346530.5:c.2043C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1983C>T
  hgvsp: ENST00000540285.1:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2152C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2152C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2172C>T
  hgvsp: ENST00000542678.1:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.804C>T
  hgvsp: ENST00000546289.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2181C>T
  hgvsp: ENST00000442028.2:c.2181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27338
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17765
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His724His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

12-123414599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414599
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414599
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 26744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2031G>A
  hgvsp: ENST00000346530.5:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2140G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2169G>A
  hgvsp: ENST00000442028.2:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2160G>A
  hgvsp: ENST00000392439.3:c.2160G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2160G>A
  hgvsp: ENST00000280560.8:c.2160G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2160G>A
  hgvsp: ENST00000542678.1:c.2160G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2140G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.792G>A
  hgvsp: ENST00000546289.1:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1971G>A
  hgvsp: ENST00000540285.1:c.1971G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25739
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22843
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln720Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-123414604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414604
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414604
    reference: chr 12
allele count: 1
allele frequency: 3.838476892369108e-5
allele num: 26052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.787G>A
  hgvsp: ENSP00000442281.1:p.Val263Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2164G>A
  hgvsp: ENSP00000394898.2:p.Val722Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2155G>A
  hgvsp: ENSP00000376234.3:p.Val719Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2135G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2155G>A
  hgvsp: ENSP00000440288.1:p.Val719Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2135G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1966G>A
  hgvsp: ENSP00000441734.1:p.Val656Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2155G>A
  hgvsp: ENSP00000280560.8:p.Val719Met
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2026G>A
  hgvsp: ENSP00000280559.7:p.Val676Met
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val719Met
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

12-123414607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414607
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414607
    reference: chr 12
allele count: 5
allele frequency: 1.937383756974582e-4
allele num: 25808
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2152G>A
  hgvsp: ENSP00000440288.1:p.Val718Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2152G>A
  hgvsp: ENSP00000280560.8:p.Val718Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2132G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2132G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2152G>A
  hgvsp: ENSP00000376234.3:p.Val718Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.784G>A
  hgvsp: ENSP00000442281.1:p.Val262Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2023G>A
  hgvsp: ENSP00000280559.7:p.Val675Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1963G>A
  hgvsp: ENSP00000441734.1:p.Val655Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2161G>A
  hgvsp: ENSP00000394898.2:p.Val721Ile
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21272
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24987
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22007
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val718Ile
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

12-123414608-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414608
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414608
    reference: chr 12
allele count: 3
allele frequency: 1.167406023815083e-4
allele num: 25698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.783C>T
  hgvsp: ENST00000546289.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2131C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2160C>T
  hgvsp: ENST00000442028.2:c.2160C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2131C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2151C>T
  hgvsp: ENST00000280560.8:c.2151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2022C>T
  hgvsp: ENST00000346530.5:c.2022C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2151C>T
  hgvsp: ENST00000542678.1:c.2151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2151C>T
  hgvsp: ENST00000392439.3:c.2151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1962C>T
  hgvsp: ENST00000540285.1:c.1962C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg717Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-123414609-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414609
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414609
    reference: chr 12
allele count: 2
allele frequency: 7.876496534341525e-5
allele num: 25392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2021G>A
  hgvsp: ENSP00000280559.7:p.Arg674His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2130G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2150G>A
  hgvsp: ENSP00000440288.1:p.Arg717His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2150G>A
  hgvsp: ENSP00000280560.8:p.Arg717His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2159G>A
  hgvsp: ENSP00000394898.2:p.Arg720His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1961G>A
  hgvsp: ENSP00000441734.1:p.Arg654His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2150G>A
  hgvsp: ENSP00000376234.3:p.Arg717His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.782G>A
  hgvsp: ENSP00000442281.1:p.Arg261His
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2130G>A
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24550
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21221
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg717His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

12-123414610-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414610
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414610
    reference: chr 12
allele count: 1
allele frequency: 3.923107100823853e-5
allele num: 25490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2149C>T
  hgvsp: ENSP00000376234.3:p.Arg717Cys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.781C>T
  hgvsp: ENSP00000442281.1:p.Arg261Cys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2149C>T
  hgvsp: ENSP00000280560.8:p.Arg717Cys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2129C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2149C>T
  hgvsp: ENSP00000440288.1:p.Arg717Cys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1960C>T
  hgvsp: ENSP00000441734.1:p.Arg654Cys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2158C>T
  hgvsp: ENSP00000394898.2:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2129C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2020C>T
  hgvsp: ENSP00000280559.7:p.Arg674Cys
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21760
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21293
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg717Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-123414616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414616
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414616
    reference: chr 12
allele count: 17
allele frequency: 6.786969019482594e-4
allele num: 25048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2123A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2123A>G
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2014A>G
  hgvsp: ENSP00000280559.7:p.Lys672Glu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2143A>G
  hgvsp: ENSP00000440288.1:p.Lys715Glu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2143A>G
  hgvsp: ENSP00000280560.8:p.Lys715Glu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2152A>G
  hgvsp: ENSP00000394898.2:p.Lys718Glu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1954A>G
  hgvsp: ENSP00000441734.1:p.Lys652Glu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.775A>G
  hgvsp: ENSP00000442281.1:p.Lys259Glu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2143A>G
  hgvsp: ENSP00000376234.3:p.Lys715Glu
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22742
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23833
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22328
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys715Glu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-123414623-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414623
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414623
    reference: chr 12
allele count: 6
allele frequency: 2.54323499491353e-4
allele num: 23592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1947G>T
  hgvsp: ENST00000540285.1:c.1947G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2145G>T
  hgvsp: ENST00000442028.2:c.2145G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.768G>T
  hgvsp: ENST00000546289.1:c.768G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2116G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2136G>T
  hgvsp: ENST00000392439.3:c.2136G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2116G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2007G>T
  hgvsp: ENST00000346530.5:c.2007G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2136G>T
  hgvsp: ENST00000280560.8:c.2136G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2136G>T
  hgvsp: ENST00000542678.1:c.2136G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22199
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23584
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18429
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 2
hgvs: p.Val712Val
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-123414625-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414625
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414625
    reference: chr 12
allele count: 17
allele frequency: 6.976935073463022e-4
allele num: 24366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2114G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2134G>T
  hgvsp: ENSP00000280560.8:p.Val712Leu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.2005G>T
  hgvsp: ENSP00000280559.7:p.Val669Leu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2143G>T
  hgvsp: ENSP00000394898.2:p.Val715Leu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.766G>T
  hgvsp: ENSP00000442281.1:p.Val256Leu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2134G>T
  hgvsp: ENSP00000376234.3:p.Val712Leu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2134G>T
  hgvsp: ENSP00000440288.1:p.Val712Leu
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2114G>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1945G>T
  hgvsp: ENSP00000441734.1:p.Val649Leu
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21646
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25017
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19289
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Val712Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

12-123414632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414632
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414632
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 23198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2136C>T
  hgvsp: ENST00000442028.2:c.2136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.1998C>T
  hgvsp: ENST00000346530.5:c.1998C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.759C>T
  hgvsp: ENST00000546289.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2107C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2127C>T
  hgvsp: ENST00000542678.1:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1938C>T
  hgvsp: ENST00000540285.1:c.1938C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2127C>T
  hgvsp: ENST00000280560.8:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2127C>T
  hgvsp: ENST00000392439.3:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2107C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19186
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2410
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu709Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-123414638-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414638
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414638
    reference: chr 12
allele count: 5
allele frequency: 2.250832808139011e-4
allele num: 22214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2121G>A
  hgvsp: ENST00000392439.3:c.2121G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.1992G>A
  hgvsp: ENST00000346530.5:c.1992G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.753G>A
  hgvsp: ENST00000546289.1:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2121G>A
  hgvsp: ENST00000542678.1:c.2121G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2101G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2130G>A
  hgvsp: ENST00000442028.2:c.2130G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1932G>A
  hgvsp: ENST00000540285.1:c.1932G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2101G>A
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2121G>A
  hgvsp: ENST00000280560.8:c.2121G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28711
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18057
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala707Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

12-123414639-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414639
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414639
    reference: chr 12
allele count: 5
allele frequency: 2.257744062133117e-4
allele num: 22146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2100C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.1991C>T
  hgvsp: ENSP00000280559.7:p.Ala664Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2120C>T
  hgvsp: ENSP00000280560.8:p.Ala707Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.752C>T
  hgvsp: ENSP00000442281.1:p.Ala251Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2120C>T
  hgvsp: ENSP00000376234.3:p.Ala707Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2129C>T
  hgvsp: ENSP00000394898.2:p.Ala710Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1931C>T
  hgvsp: ENSP00000441734.1:p.Ala644Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2120C>T
  hgvsp: ENSP00000440288.1:p.Ala707Val
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2100C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17811
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28214
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13800
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala707Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

12-123414641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414641
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414641
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 20894
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2118C>T
  hgvsp: ENST00000542678.1:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.1989C>T
  hgvsp: ENST00000346530.5:c.1989C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2098C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2118C>T
  hgvsp: ENST00000280560.8:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.750C>T
  hgvsp: ENST00000546289.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2127C>T
  hgvsp: ENST00000442028.2:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2118C>T
  hgvsp: ENST00000392439.3:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1929C>T
  hgvsp: ENST00000540285.1:c.1929C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2098C>T
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30144
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His706His
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

12-123414650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414650
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414650
    reference: chr 12
allele count: 3
allele frequency: 1.446759259259259e-4
allele num: 20736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.741C>T
  hgvsp: ENST00000546289.1:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2109C>T
  hgvsp: ENST00000542678.1:c.2109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1920C>T
  hgvsp: ENST00000540285.1:c.1920C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2109C>T
  hgvsp: ENST00000280560.8:c.2109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2089C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.1980C>T
  hgvsp: ENST00000346530.5:c.1980C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2118C>T
  hgvsp: ENST00000442028.2:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2089C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2109C>T
  hgvsp: ENST00000392439.3:c.2109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29781
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr703Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

12-123414651-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123414651
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123414651
    reference: chr 12
allele count: 2
allele frequency: 9.744689144416293e-5
allele num: 20524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456375
  ensembl transcript: ENST00000442833
  gene symbol: ABCB9
  hgvsc: ENST00000442833.2:c.2040+2088C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000441734
  ensembl transcript: ENST00000540285
  gene symbol: ABCB9
  hgvsc: ENST00000540285.1:c.1919C>T
  hgvsp: ENSP00000441734.1:p.Thr640Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280560
  ensembl transcript: ENST00000280560
  gene symbol: ABCB9
  hgvsc: ENST00000280560.8:c.2108C>T
  hgvsp: ENSP00000280560.8:p.Thr703Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000456813
  ensembl transcript: ENST00000344275
  gene symbol: ABCB9
  hgvsc: ENST00000344275.7:c.2040+2088C>T
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000280559
  ensembl transcript: ENST00000346530
  gene symbol: ABCB9
  hgvsc: ENST00000346530.5:c.1979C>T
  hgvsp: ENSP00000280559.7:p.Thr660Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000442281
  ensembl transcript: ENST00000546289
  gene symbol: ABCB9
  hgvsc: ENST00000546289.1:c.740C>T
  hgvsp: ENSP00000442281.1:p.Thr247Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000394898
  ensembl transcript: ENST00000442028
  gene symbol: ABCB9
  hgvsc: ENST00000442028.2:c.2117C>T
  hgvsp: ENSP00000394898.2:p.Thr706Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000376234
  ensembl transcript: ENST00000392439
  gene symbol: ABCB9
  hgvsc: ENST00000392439.3:c.2108C>T
  hgvsp: ENSP00000376234.3:p.Thr703Ile
  variant of: http://identifiers.org/hgnc/50
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150967
  ensembl protein: ENSP00000440288
  ensembl transcript: ENST00000542678
  gene symbol: ABCB9
  hgvsc: ENST00000542678.1:c.2108C>T
  hgvsp: ENSP00000440288.1:p.Thr703Ile
  variant of: http://identifiers.org/hgnc/50
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29892
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr703Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39030
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.691474966170501e-4
allele num: 5912
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 8.31617e5

VQSLOD
type: SiteQuality
SIO_000300: 1.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.532e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.564497102118275e-5
allele num: 38994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7366
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.3006e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.282e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.303e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.51e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.662690382362339e-5
allele num: 37556
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.333e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.147e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 8.19744e5

VQSLOD
type: SiteQuality
SIO_000300: -1.241e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.085e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.82e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 9.25e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.843657817109145e-4
allele num: 5424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34916
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

QD
type: SiteQuality
SIO_000300: 9.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.919e0

VQSLOD
type: SiteQuality
SIO_000300: -7.381e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.07076e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.164e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.019688368160406e-5
allele num: 33116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.079e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.3e1

DP
type: SiteQuality
SIO_000300: 8.01377e5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26842
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.412429378531073e-4
allele num: 7080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.048e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.367e0

DP
type: SiteQuality
SIO_000300: 7.95857e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.553e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.58e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.202e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

DP
type: SiteQuality
SIO_000300: 2.68354e5

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 3.445e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.94e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

DP
type: SiteQuality
SIO_000300: 3.43341e5

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 4.392386530014641e-3
allele num: 2732
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 9.900990099009901e-2
allele num: 202
num of homozygotes: 2

East Asian
type: Population
allele count: 2
allele frequency: 1.492537313432836e-2
allele num: 134
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 8.474576271186441e-3
allele num: 118
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 1.332622601279318e-3
allele num: 7504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 3.43504e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

QD
type: SiteQuality
SIO_000300: 1.434e1

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2539
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4606
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17882
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.540521314973833e-5
allele num: 39362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.763e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.90062e5

QD
type: SiteQuality
SIO_000300: 1.276e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

GenotypeQuality
all individuals: 1690
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19270
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4302
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.094762584063582e-5
allele num: 39256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.526e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 6.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 7.23e0

DP
type: SiteQuality
SIO_000300: 7.07299e5

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5336
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.967729240456513e-4
allele num: 5082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2314
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.526e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 7.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 6.092e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

DP
type: SiteQuality
SIO_000300: 7.07299e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 6107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 14440
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2555
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5250
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.202049311559398e-4
allele num: 6246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2382
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.70489e5

QD
type: SiteQuality
SIO_000300: 7.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

GenotypeQuality
all individuals: 270
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5870
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22553
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 783
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.202049311559398e-4
allele num: 6246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5428
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.87741e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

FS
type: SiteQuality
SIO_000300: 2.309e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.18e1

GenotypeQuality
all individuals: 283
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3609
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2879
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14855
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 954
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.75e1
variant carriers: 53

GenotypeQuality
all individuals: 694
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.860960457548565e-5
allele num: 40564
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.739715781600598e-4
allele num: 5348
num of homozygotes: 0

East Asian
type: Population
allele count: 45
allele frequency: 8.23271130625686e-3
allele num: 5466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2418
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 8.972633467922835e-4
allele num: 4458
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 5.405405405405406e-3
allele num: 370
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 5.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.94822e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 1.036e1

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 845
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 250
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5474
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5528
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 7.304601899196494e-4
allele num: 5476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 7.068688148978696e-4
allele num: 41026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.461e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.026e0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 8.069e5

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

GenotypeQuality
all individuals: 2415
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
all individuals: 625
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variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23810
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 19869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
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variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.395783421178726e-5
allele num: 41740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5594
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.272e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 8.41883e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.38e-1

FS
type: SiteQuality
SIO_000300: 2.699e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

GenotypeQuality
all individuals: 2158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 509
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.535615523982073e-5
allele num: 41948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4760
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

DP
type: SiteQuality
SIO_000300: 8.53089e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

QD
type: SiteQuality
SIO_000300: 9.18e0

GenotypeQuality
all individuals: 215
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 519
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variant carriers: 0

GenotypeQuality
all individuals: 20520
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 1

GenotypeQuality
all individuals: 4134
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
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GenotypeQuality
all individuals: 759
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.025931928687196e-4
allele num: 4936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5690
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.376e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

MQ
type: SiteQuality
SIO_000300: 5.906e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

FS
type: SiteQuality
SIO_000300: 4.379e0

DP
type: SiteQuality
SIO_000300: 8.62637e5

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
all individuals: 3725
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 400
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21280
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 744
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.35393813850572e-5
allele num: 42482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 9.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.61e0

FS
type: SiteQuality
SIO_000300: 6.425e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

DP
type: SiteQuality
SIO_000300: 8.72469e5

GenotypeQuality
all individuals: 3608
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26007
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GenotypeQuality
all individuals: 332
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GenotypeQuality
all individuals: 713
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
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GenotypeQuality
all individuals: 1703
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GenotypeQuality
all individuals: 822
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 521
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variant carriers: 0

GenotypeQuality
all individuals: 20664
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5142
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.628201172477631e-4
allele num: 6482
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

DP
type: SiteQuality
SIO_000300: 8.71685e5

MQ
type: SiteQuality
SIO_000300: 5.983e1

FS
type: SiteQuality
SIO_000300: 3.395e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.87e-1

GenotypeQuality
all individuals: 20725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3529
bin: 7.5e0
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GenotypeQuality
all individuals: 407
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 765
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 432
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 9.464767403341063e-5
allele num: 42262
num of homozygotes: 0

South Asian
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Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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East Asian
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allele num: 5754
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Latino
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African
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Other
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South Asian
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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FS
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 2.377782004945787e-5
allele num: 42056
num of homozygotes: 0

Latino
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allele num: 5646
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 4.174397031539889e-3
allele num: 6468
num of homozygotes: 0

Other
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: -2.7e-1

VQSLOD
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

Other
type: Population
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allele num: 396
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.372929618907503e-5
allele num: 42142
num of homozygotes: 0

South Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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African
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East Asian
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allele num: 5654
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European (Finnish)
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 41632
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East Asian
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Latino
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Other
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African
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European (Finnish)
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South Asian
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QD
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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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
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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Other
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.723034509919756e-4
allele num: 40626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2450
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.717032967032967e-4
allele num: 5824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.47759e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

FS
type: SiteQuality
SIO_000300: 5.322e0

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.098e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 181
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2162
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.857142857142857e-3
allele num: 350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4770
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.76081233546446e-4
allele num: 5318
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

FS
type: SiteQuality
SIO_000300: 1.855e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

DP
type: SiteQuality
SIO_000300: 7.92986e5

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.155e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 1.932367149758454e-3
allele num: 2070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 4.599318218711109e-4
allele num: 36962
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.177e1

QD
type: SiteQuality
SIO_000300: 3.55e0

DP
type: SiteQuality
SIO_000300: 7.73261e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.061e0

FS
type: SiteQuality
SIO_000300: 2.569e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-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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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.448800270361608e-5
allele num: 35508
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.746419839329375e-4
allele num: 5726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 6.871278057718735e-4
allele num: 4366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

FS
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.056e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

DP
type: SiteQuality
SIO_000300: 7.48803e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 709
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GenotypeQuality
all individuals: 22
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.94883997620464e-5
allele num: 33620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.994e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

QD
type: SiteQuality
SIO_000300: 6.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.747e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 7.17051e5

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 370
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GenotypeQuality
all individuals: 213
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 441
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6920
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.453385672227674e-4
allele num: 4076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33670
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-2

DP
type: SiteQuality
SIO_000300: 7.19739e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.352e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.402131239484016e-4
allele num: 7132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.144e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.402e0

QD
type: SiteQuality
SIO_000300: 2.791e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.11755e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 1
allele frequency: 1.836884643644379e-4
allele num: 5444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7198
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.07154e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 4.89e0

VQSLOD
type: SiteQuality
SIO_000300: -1.859e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 161
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 2.906976744186046e-3
allele num: 344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3732
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

FS
type: SiteQuality
SIO_000300: 3.424e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

DP
type: SiteQuality
SIO_000300: 6.77903e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.186e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 122
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GenotypeQuality
all individuals: 3223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30530
bin: 2.25e1
variant carriers: 1

South Asian
type: Population
allele count: 18
allele frequency: 2.415458937198068e-3
allele num: 7452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 6.920415224913495e-4
allele num: 2890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

FS
type: SiteQuality
SIO_000300: 7.707e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.18e-2

QD
type: SiteQuality
SIO_000300: 1.102e1

DP
type: SiteQuality
SIO_000300: 6.18496e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 694
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5333
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9609
bin: 7.5e0
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GenotypeQuality
all individuals: 405
bin: 4.25e1
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GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 616
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.133105802047782e-4
allele num: 4688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.848818412747287e-5
allele num: 25982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 8.47457627118644e-4
allele num: 1180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2862
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

QD
type: SiteQuality
SIO_000300: 1.092e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

FS
type: SiteQuality
SIO_000300: 1.0609e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.114e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e-1

DP
type: SiteQuality
SIO_000300: 6.1551e5

GenotypeQuality
all individuals: 393
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30008
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1141
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.218917601170161e-4
allele num: 24612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4550
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.308557969118032e-4
allele num: 7642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

FS
type: SiteQuality
SIO_000300: 1.627e0

QD
type: SiteQuality
SIO_000300: 1.37e1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

DP
type: SiteQuality
SIO_000300: 6.07274e5

GenotypeQuality
all individuals: 329
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
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variant carriers: 0

GenotypeQuality
all individuals: 2103
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variant carriers: 0

GenotypeQuality
all individuals: 5900
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variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10050
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GenotypeQuality
all individuals: 381
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GenotypeQuality
all individuals: 2417
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variant carriers: 0

GenotypeQuality
all individuals: 31031
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1079
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.99e-1

FS
type: SiteQuality
SIO_000300: 3.089e0

DP
type: SiteQuality
SIO_000300: 6.09347e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 53
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
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variant carriers: 0

GenotypeQuality
all individuals: 11301
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GenotypeQuality
all individuals: 30092
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variant carriers: 0

GenotypeQuality
all individuals: 2263
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variant carriers: 0

GenotypeQuality
all individuals: 709
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variant carriers: 0

GenotypeQuality
all individuals: 2236
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variant carriers: 0

GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 259
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GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 6305
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variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2178
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.287282708142727e-4
allele num: 4372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22772
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.93709e5

FS
type: SiteQuality
SIO_000300: 1.337e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.146e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

VQSLOD
type: SiteQuality
SIO_000300: -1.564e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.366e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
all individuals: 6379
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.5e0
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GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 6.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.62e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 5.82775e5

VQSLOD
type: SiteQuality
SIO_000300: -1.114e0

FS
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 28600
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12354
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GenotypeQuality
all individuals: 137
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GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 1589
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variant carriers: 0

GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 3204
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 9.25925925925926e-4
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21074
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.012e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.8183e5

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

GenotypeQuality
all individuals: 28983
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 2303
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
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GenotypeQuality
all individuals: 174
bin: 4.25e1
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GenotypeQuality
all individuals: 6828
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.461841457410143e-4
allele num: 4062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.964750273061265e-5
allele num: 20142
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 5.78934e5

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.089e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

GenotypeQuality
all individuals: 982
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28067
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variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 13177
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 33
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variant carriers: 2

GenotypeQuality
all individuals: 157
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GenotypeQuality
all individuals: 1343
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GenotypeQuality
all individuals: 1823
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GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 580
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.337135614702154e-4
allele num: 1578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.700962250185048e-4
allele num: 2702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.12e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.51e-1

FS
type: SiteQuality
SIO_000300: 5.388e0

QD
type: SiteQuality
SIO_000300: 7.55e0

DP
type: SiteQuality
SIO_000300: 5.74761e5

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2492
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 1462
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 5.286529921759357e-5
allele num: 18916
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -1.007e0

BaseQRankSum
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SIO_000300: -2.793e0

QD
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InbreedingCoeff
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SIO_000300: -2.75e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 6.892e0

DP
type: SiteQuality
SIO_000300: 5.67967e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16636
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 1216
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.48832e5

BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.016e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16614
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 3674
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 3.495688650664181e-4
allele num: 8582
num of homozygotes: 1

Latino
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allele frequency: 0.0e0
allele num: 1216
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 4.557885141294439e-4
allele num: 2194
num of homozygotes: 0

Other
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.67e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: -2.266e0

FS
type: SiteQuality
SIO_000300: 1.5243e1

QD
type: SiteQuality
SIO_000300: 1.218e1

DP
type: SiteQuality
SIO_000300: 5.49295e5

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3650
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 5.45151e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.105e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

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

South Asian
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allele count: 1
allele frequency: 1.181753722524226e-4
allele num: 8462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.296176279974077e-4
allele num: 15430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3536
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1972
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.40727e5

VQSLOD
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.23e-2

FS
type: SiteQuality
SIO_000300: 1.387e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3462
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 14340
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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FS
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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Other
type: Population
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African
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European (Finnish)
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
type: Population
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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African
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Other
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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QD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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MQ
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
allele num: 1388
num of homozygotes: 0

African
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allele frequency: 3.121098626716604e-4
allele num: 3204
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 12120
num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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FS
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QD
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ClippingRankSum
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DP
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 9.375e-4
allele num: 3200
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 1.675884028825205e-4
allele num: 11934
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

QD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 8.427439743805832e-5
allele num: 11866
num of homozygotes: 0

South Asian
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allele frequency: 2.460629921259842e-4
allele num: 8128
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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VQSLOD
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QD
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
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SIO_000300: -8.32e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 1.457725947521866e-3
allele num: 686
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 4.761904761904762e-3
allele num: 210
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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QD
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MQRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 2.384e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.16e-2

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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European (Non-Finnish)
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allele num: 11440
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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DP
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FS
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.75834e5

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 2922
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 192
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -5.15e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.5488e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -5.5e-1

ReadPosRankSum
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

GenotypeQuality
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bin: 9.25e1
variant carriers: 2

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 3.793626707132018e-4
allele num: 7908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 942
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.952569169960474e-3
allele num: 506
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.42925e5

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.169e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 942
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.05761316872428e-3
allele num: 486
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

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

African
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allele frequency: 1.072961373390558e-3
allele num: 2796
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.265822784810127e-4
allele num: 7900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.41008e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.239e0

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.48e-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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele num: 410
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East Asian
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South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.82e-2

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.494e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 4.26249e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 7824
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European (Non-Finnish)
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allele frequency: 2.270147559591373e-4
allele num: 8810
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Latino
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East Asian
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Other
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African
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allele num: 2624
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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DP
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QD
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

African
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East Asian
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South Asian
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allele frequency: 2.566735112936345e-4
allele num: 7792
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European (Non-Finnish)
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Other
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Latino
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ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
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FS
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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