7-150732666-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732666
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732666
    reference: chr 7
allele count: 1
allele frequency: 8.78966335589347e-6
allele num: 113770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*368-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.766-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.817-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.766-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.766-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*409-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.766-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*333-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.877-2A>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.502-2A>T
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
hgvs: c.766-2A>T
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-150732674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732674
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732674
    reference: chr 7
allele count: 4
allele frequency: 3.485049139192863e-5
allele num: 114776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.772C>T
  hgvsp: ENSP00000419891.1:p.Arg258Ter
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.772C>T
  hgvsp: ENSP00000351717.4:p.Arg258Ter
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*415C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.508C>T
  hgvsp: ENSP00000438776.1:p.Arg170Ter
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*374C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.823C>T
  hgvsp: ENSP00000297504.6:p.Arg275Ter
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.772C>T
  hgvsp: ENSP00000419558.1:p.Arg258Ter
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.883C>T
  hgvsp: ENSP00000348353.4:p.Arg295Ter
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*339C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.772C>T
  hgvsp: ENSP00000418271.1:p.Arg258Ter
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg258Ter
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

7-150732675-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732675
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732675
    reference: chr 7
allele count: 252
allele frequency: 2.185602775368604e-3
allele num: 115300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*375G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.773G>A
  hgvsp: ENSP00000418271.1:p.Arg258Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.773G>A
  hgvsp: ENSP00000351717.4:p.Arg258Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.884G>A
  hgvsp: ENSP00000348353.4:p.Arg295Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*416G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*340G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.509G>A
  hgvsp: ENSP00000438776.1:p.Arg170Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.773G>A
  hgvsp: ENSP00000419558.1:p.Arg258Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.824G>A
  hgvsp: ENSP00000297504.6:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.773G>A
  hgvsp: ENSP00000419891.1:p.Arg258Gln
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15056
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 9.75e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg258Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

7-150732681-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732681
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732681
    reference: chr 7
allele count: 2
allele frequency: 1.720400509238551e-5
allele num: 116252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.779G>C
  hgvsp: ENSP00000418271.1:p.Cys260Ser
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*381G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.515G>C
  hgvsp: ENSP00000438776.1:p.Cys172Ser
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.779G>C
  hgvsp: ENSP00000351717.4:p.Cys260Ser
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*346G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.830G>C
  hgvsp: ENSP00000297504.6:p.Cys277Ser
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.890G>C
  hgvsp: ENSP00000348353.4:p.Cys297Ser
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.779G>C
  hgvsp: ENSP00000419558.1:p.Cys260Ser
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*422G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.779G>C
  hgvsp: ENSP00000419891.1:p.Cys260Ser
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys260Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-150732700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732700
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732700
    reference: chr 7
allele count: 1
allele frequency: 8.423180592991915e-6
allele num: 118720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.909C>T
  hgvsp: ENST00000356058.4:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.849C>T
  hgvsp: ENST00000297504.6:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.798C>T
  hgvsp: ENST00000477719.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.798C>T
  hgvsp: ENST00000477092.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.798C>T
  hgvsp: ENST00000498578.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*441C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*365C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.798C>T
  hgvsp: ENST00000358849.4:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.534C>T
  hgvsp: ENST00000542328.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys266Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

7-150732712-GTCCATGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732712
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732705
    reference: chr 7
allele count: 2
allele frequency: 1.671625823275718e-5
allele num: 119644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.548_554delCCATGCT
  hgvsp: ENSP00000438776.1:p.Ser183CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.812_818delCCATGCT
  hgvsp: ENSP00000419558.1:p.Ser271CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.863_869delCCATGCT
  hgvsp: ENSP00000297504.6:p.Ser288CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.923_929delCCATGCT
  hgvsp: ENSP00000348353.4:p.Ser308CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.812_818delCCATGCT
  hgvsp: ENSP00000419891.1:p.Ser271CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*414_*420delCCATGCT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.812_818delCCATGCT
  hgvsp: ENSP00000351717.4:p.Ser271CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.812_818delCCATGCT
  hgvsp: ENSP00000418271.1:p.Ser271CysfsTer9
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*455_*461delCCATGCT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*379_*385delCCATGCT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.9_15delCCATGCT
  hgvsp: ENSP00000420162.1:p.Ser4CysfsTer9
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser271CysfsTer9
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: GTCCATGC
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-150732723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732723
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732723
    reference: chr 7
allele count: 2
allele frequency: 1.663035705376594e-5
allele num: 120262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*388C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.821C>T
  hgvsp: ENSP00000419891.1:p.Ser274Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.557C>T
  hgvsp: ENSP00000438776.1:p.Ser186Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.821C>T
  hgvsp: ENSP00000419558.1:p.Ser274Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.932C>T
  hgvsp: ENSP00000348353.4:p.Ser311Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.821C>T
  hgvsp: ENSP00000418271.1:p.Ser274Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*464C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.821C>T
  hgvsp: ENSP00000351717.4:p.Ser274Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.872C>T
  hgvsp: ENSP00000297504.6:p.Ser291Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*423C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.18C>T
  hgvsp: ENSP00000420162.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser274Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

7-150732724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732724
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732724
    reference: chr 7
allele count: 2
allele frequency: 1.660908849322349e-5
allele num: 120416
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.822G>A
  hgvsp: ENST00000358849.4:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.558G>A
  hgvsp: ENST00000542328.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.822G>A
  hgvsp: ENST00000477719.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.822G>A
  hgvsp: ENST00000477092.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.19G>A
  hgvsp: ENST00000491920.1:c.19G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.822G>A
  hgvsp: ENST00000498578.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*465G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.933G>A
  hgvsp: ENST00000356058.4:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*424G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.873G>A
  hgvsp: ENST00000297504.6:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*389G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser274Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

7-150732724-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732724
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732724
    reference: chr 7
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.933G>C
  hgvsp: ENST00000356058.4:c.933G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.19G>C
  hgvsp: ENST00000491920.1:c.19G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.822G>C
  hgvsp: ENST00000477719.1:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*389G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.873G>C
  hgvsp: ENST00000297504.6:c.873G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.822G>C
  hgvsp: ENST00000498578.1:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.822G>C
  hgvsp: ENST00000477092.1:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.558G>C
  hgvsp: ENST00000542328.1:c.558G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.822G>C
  hgvsp: ENST00000358849.4:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*465G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*424G>C
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser274Ser
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

7-150732725-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732725
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732725
    reference: chr 7
allele count: 2
allele frequency: 1.660715768496222e-5
allele num: 120430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.823A>G
  hgvsp: ENSP00000419891.1:p.Thr275Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.823A>G
  hgvsp: ENSP00000418271.1:p.Thr275Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.20A>G
  hgvsp: ENSP00000420162.1:p.Thr8Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*425A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.823A>G
  hgvsp: ENSP00000351717.4:p.Thr275Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.934A>G
  hgvsp: ENSP00000348353.4:p.Thr312Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.874A>G
  hgvsp: ENSP00000297504.6:p.Thr292Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.823A>G
  hgvsp: ENSP00000419558.1:p.Thr275Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*390A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*466A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.559A>G
  hgvsp: ENSP00000438776.1:p.Thr187Ala
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr275Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

7-150732728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732728
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732728
    reference: chr 7
allele count: 2
allele frequency: 1.659255326209597e-5
allele num: 120536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*393C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.826C>T
  hgvsp: ENSP00000351717.4:p.Arg276Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.937C>T
  hgvsp: ENSP00000348353.4:p.Arg313Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.826C>T
  hgvsp: ENSP00000418271.1:p.Arg276Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.877C>T
  hgvsp: ENSP00000297504.6:p.Arg293Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.23C>T
  hgvsp: ENSP00000420162.1:p.Arg9Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.826C>T
  hgvsp: ENSP00000419891.1:p.Arg276Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*428C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.826C>T
  hgvsp: ENSP00000419558.1:p.Arg276Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.562C>T
  hgvsp: ENSP00000438776.1:p.Arg188Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*469C>T
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg276Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

7-150732729-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732729
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732729
    reference: chr 7
allele count: 5
allele frequency: 4.14696856597827e-5
allele num: 120570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*470G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*429G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.563G>A
  hgvsp: ENSP00000438776.1:p.Arg188His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.24G>A
  hgvsp: ENSP00000420162.1:p.Arg9His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.827G>A
  hgvsp: ENSP00000419558.1:p.Arg276His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.938G>A
  hgvsp: ENSP00000348353.4:p.Arg313His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.878G>A
  hgvsp: ENSP00000297504.6:p.Arg293His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.827G>A
  hgvsp: ENSP00000351717.4:p.Arg276His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.827G>A
  hgvsp: ENSP00000418271.1:p.Arg276His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*394G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.827G>A
  hgvsp: ENSP00000419891.1:p.Arg276His
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg276His
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

7-150732729-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732729
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732729
    reference: chr 7
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.827G>C
  hgvsp: ENSP00000418271.1:p.Arg276Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.827G>C
  hgvsp: ENSP00000419558.1:p.Arg276Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.827G>C
  hgvsp: ENSP00000419891.1:p.Arg276Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.878G>C
  hgvsp: ENSP00000297504.6:p.Arg293Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.938G>C
  hgvsp: ENSP00000348353.4:p.Arg313Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.827G>C
  hgvsp: ENSP00000351717.4:p.Arg276Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.24G>C
  hgvsp: ENSP00000420162.1:p.Arg9Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*470G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.563G>C
  hgvsp: ENSP00000438776.1:p.Arg188Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*429G>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*394G>C
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg276Pro
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: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-150732735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732735
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732735
    reference: chr 7
allele count: 6
allele frequency: 4.970673029128144e-5
allele num: 120708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.569C>T
  hgvsp: ENSP00000438776.1:p.Thr190Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.833C>T
  hgvsp: ENSP00000418271.1:p.Thr278Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.833C>T
  hgvsp: ENSP00000351717.4:p.Thr278Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.944C>T
  hgvsp: ENSP00000348353.4:p.Thr315Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.884C>T
  hgvsp: ENSP00000297504.6:p.Thr295Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.833C>T
  hgvsp: ENSP00000419891.1:p.Thr278Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*435C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.833C>T
  hgvsp: ENSP00000419558.1:p.Thr278Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*476C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.30C>T
  hgvsp: ENSP00000420162.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16669
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Thr278Met
num of homozygotes: 1
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

7-150732736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732736
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732736
    reference: chr 7
allele count: 9
allele frequency: 7.452922373672965e-5
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.834G>A
  hgvsp: ENST00000477719.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.570G>A
  hgvsp: ENST00000542328.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*477G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.834G>A
  hgvsp: ENST00000358849.4:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.834G>A
  hgvsp: ENST00000498578.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.945G>A
  hgvsp: ENST00000356058.4:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.31G>A
  hgvsp: ENST00000491920.1:c.31G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.834G>A
  hgvsp: ENST00000477092.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.885G>A
  hgvsp: ENST00000297504.6:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*436G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*401G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr278Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-150732736-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732736
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732736
    reference: chr 7
allele count: 5
allele frequency: 4.140512429818314e-5
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.570G>T
  hgvsp: ENST00000542328.1:c.570G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.31G>T
  hgvsp: ENST00000491920.1:c.31G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.885G>T
  hgvsp: ENST00000297504.6:c.885G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*401G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.834G>T
  hgvsp: ENST00000358849.4:c.834G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.945G>T
  hgvsp: ENST00000356058.4:c.945G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.834G>T
  hgvsp: ENST00000498578.1:c.834G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.834G>T
  hgvsp: ENST00000477092.1:c.834G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.834G>T
  hgvsp: ENST00000477719.1:c.834G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*477G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*436G>T
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr278Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-150732741-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732741
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732741
    reference: chr 7
allele count: 2
allele frequency: 1.654861984510492e-5
allele num: 120856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.575T>C
  hgvsp: ENSP00000438776.1:p.Leu192Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.950T>C
  hgvsp: ENSP00000348353.4:p.Leu317Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*406T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.839T>C
  hgvsp: ENSP00000418271.1:p.Leu280Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.890T>C
  hgvsp: ENSP00000297504.6:p.Leu297Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.839T>C
  hgvsp: ENSP00000419558.1:p.Leu280Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*482T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.839T>C
  hgvsp: ENSP00000351717.4:p.Leu280Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*441T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.839T>C
  hgvsp: ENSP00000419891.1:p.Leu280Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.36T>C
  hgvsp: ENSP00000420162.1:p.Leu13Pro
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu280Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

7-150732749-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732749
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732749
    reference: chr 7
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*414G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.958G>A
  hgvsp: ENSP00000348353.4:p.Val320Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.847G>A
  hgvsp: ENSP00000418271.1:p.Val283Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.44G>A
  hgvsp: ENSP00000420162.1:p.Val16Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.847G>A
  hgvsp: ENSP00000419891.1:p.Val283Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*449G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.847G>A
  hgvsp: ENSP00000351717.4:p.Val283Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.898G>A
  hgvsp: ENSP00000297504.6:p.Val300Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.847G>A
  hgvsp: ENSP00000419558.1:p.Val283Met
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.583G>A
  hgvsp: ENSP00000438776.1:p.Val195Met
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val283Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-150732750-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732750
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732750
    reference: chr 7
allele count: 2
allele frequency: 1.653986106516705e-5
allele num: 120920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.848T>G
  hgvsp: ENSP00000419891.1:p.Val283Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.45T>G
  hgvsp: ENSP00000420162.1:p.Val16Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.959T>G
  hgvsp: ENSP00000348353.4:p.Val320Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.848T>G
  hgvsp: ENSP00000351717.4:p.Val283Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*491T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.848T>G
  hgvsp: ENSP00000419558.1:p.Val283Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.584T>G
  hgvsp: ENSP00000438776.1:p.Val195Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.899T>G
  hgvsp: ENSP00000297504.6:p.Val300Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.848T>G
  hgvsp: ENSP00000418271.1:p.Val283Gly
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*450T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*415T>G
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val283Gly
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-150732751-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732751
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732751
    reference: chr 7
allele count: 1
allele frequency: 8.270204108637402e-6
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*492G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.849G>A
  hgvsp: ENST00000477719.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.849G>A
  hgvsp: ENST00000477092.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.960G>A
  hgvsp: ENST00000356058.4:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.900G>A
  hgvsp: ENST00000297504.6:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.849G>A
  hgvsp: ENST00000498578.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.585G>A
  hgvsp: ENST00000542328.1:c.585G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*416G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*451G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.46G>A
  hgvsp: ENST00000491920.1:c.46G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.849G>A
  hgvsp: ENST00000358849.4:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val283Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

7-150732752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732752
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732752
    reference: chr 7
allele count: 1
allele frequency: 8.269793751343841e-6
allele num: 120922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.901G>A
  hgvsp: ENSP00000297504.6:p.Ala301Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.961G>A
  hgvsp: ENSP00000348353.4:p.Ala321Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.586G>A
  hgvsp: ENSP00000438776.1:p.Ala196Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.850G>A
  hgvsp: ENSP00000418271.1:p.Ala284Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.850G>A
  hgvsp: ENSP00000419891.1:p.Ala284Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*417G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.850G>A
  hgvsp: ENSP00000419558.1:p.Ala284Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*452G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.850G>A
  hgvsp: ENSP00000351717.4:p.Ala284Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.47G>A
  hgvsp: ENSP00000420162.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*493G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala284Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-150732757-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732757
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732757
    reference: chr 7
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.52A>C
  hgvsp: ENST00000491920.1:c.52A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.591A>C
  hgvsp: ENST00000542328.1:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*422A>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*498A>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.906A>C
  hgvsp: ENST00000297504.6:c.906A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.855A>C
  hgvsp: ENST00000358849.4:c.855A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.855A>C
  hgvsp: ENST00000477092.1:c.855A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.855A>C
  hgvsp: ENST00000498578.1:c.855A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.855A>C
  hgvsp: ENST00000477719.1:c.855A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.966A>C
  hgvsp: ENST00000356058.4:c.966A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*457A>C
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr285Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/7-150732758-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732758
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732758
    reference: chr 7
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.967C>A
  hgvsp: ENSP00000348353.4:p.Pro323Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.907C>A
  hgvsp: ENSP00000297504.6:p.Pro303Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.856C>A
  hgvsp: ENSP00000418271.1:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*499C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.856C>A
  hgvsp: ENSP00000351717.4:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.856C>A
  hgvsp: ENSP00000419891.1:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*423C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*458C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.592C>A
  hgvsp: ENSP00000438776.1:p.Pro198Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.856C>A
  hgvsp: ENSP00000419558.1:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.53C>A
  hgvsp: ENSP00000420162.1:p.Pro19Thr
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro286Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum

7-150732771-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732771
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732771
    reference: chr 7
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.605G>A
  hgvsp: ENSP00000438776.1:p.Gly202Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.920G>A
  hgvsp: ENSP00000297504.6:p.Gly307Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.869G>A
  hgvsp: ENSP00000418271.1:p.Gly290Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.66G>A
  hgvsp: ENSP00000420162.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*512G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*471G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*436G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.869G>A
  hgvsp: ENSP00000419891.1:p.Gly290Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.980G>A
  hgvsp: ENSP00000348353.4:p.Gly327Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.869G>A
  hgvsp: ENSP00000419558.1:p.Gly290Glu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.869G>A
  hgvsp: ENSP00000351717.4:p.Gly290Glu
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly290Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/7-150732781-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732781
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732781
    reference: chr 7
allele count: 2
allele frequency: 1.652810604432838e-5
allele num: 121006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.879C>A
  hgvsp: ENST00000477092.1:c.879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*522C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*446C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.615C>A
  hgvsp: ENST00000542328.1:c.615C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.76C>A
  hgvsp: ENST00000491920.1:c.76C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.879C>A
  hgvsp: ENST00000498578.1:c.879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.930C>A
  hgvsp: ENST00000297504.6:c.930C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.879C>A
  hgvsp: ENST00000358849.4:c.879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*481C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.879C>A
  hgvsp: ENST00000477719.1:c.879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.990C>A
  hgvsp: ENST00000356058.4:c.990C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr293Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-150732783-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732783
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732783
    reference: chr 7
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.78T>C
  hgvsp: ENSP00000420162.1:p.Leu27Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*483T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.932T>C
  hgvsp: ENSP00000297504.6:p.Leu311Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*524T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.881T>C
  hgvsp: ENSP00000418271.1:p.Leu294Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.992T>C
  hgvsp: ENSP00000348353.4:p.Leu331Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.617T>C
  hgvsp: ENSP00000438776.1:p.Leu206Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*448T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.881T>C
  hgvsp: ENSP00000419558.1:p.Leu294Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.881T>C
  hgvsp: ENSP00000351717.4:p.Leu294Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.881T>C
  hgvsp: ENSP00000419891.1:p.Leu294Pro
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu294Pro
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: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

7-150732784-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732784
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732784
    reference: chr 7
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.882G>A
  hgvsp: ENST00000498578.1:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.933G>A
  hgvsp: ENST00000297504.6:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*525G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.993G>A
  hgvsp: ENST00000356058.4:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.618G>A
  hgvsp: ENST00000542328.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*449G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.882G>A
  hgvsp: ENST00000477719.1:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.882G>A
  hgvsp: ENST00000358849.4:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.79G>A
  hgvsp: ENST00000491920.1:c.79G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.882G>A
  hgvsp: ENST00000477092.1:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*484G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu294Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-150732787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732787
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732787
    reference: chr 7
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.885G>A
  hgvsp: ENSP00000419891.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.885G>A
  hgvsp: ENSP00000418271.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*452G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.82G>A
  hgvsp: ENSP00000420162.1:p.Met28Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.885G>A
  hgvsp: ENSP00000419558.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.996G>A
  hgvsp: ENSP00000348353.4:p.Met332Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.621G>A
  hgvsp: ENSP00000438776.1:p.Met207Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.936G>A
  hgvsp: ENSP00000297504.6:p.Met312Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*528G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.885G>A
  hgvsp: ENSP00000351717.4:p.Met295Ile
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*487G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met295Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

7-150732789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732789
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732789
    reference: chr 7
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.998G>A
  hgvsp: ENSP00000348353.4:p.Gly333Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.887G>A
  hgvsp: ENSP00000418271.1:p.Gly296Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.887G>A
  hgvsp: ENSP00000419891.1:p.Gly296Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*530G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.623G>A
  hgvsp: ENSP00000438776.1:p.Gly208Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*454G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.84G>A
  hgvsp: ENSP00000420162.1:p.Gly29Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.938G>A
  hgvsp: ENSP00000297504.6:p.Gly313Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.887G>A
  hgvsp: ENSP00000351717.4:p.Gly296Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.887G>A
  hgvsp: ENSP00000419558.1:p.Gly296Asp
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*489G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly296Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

7-150732789-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732789
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732789
    reference: chr 7
allele count: 10
allele frequency: 8.26255081468751e-5
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.998G>T
  hgvsp: ENSP00000348353.4:p.Gly333Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.887G>T
  hgvsp: ENSP00000419891.1:p.Gly296Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*454G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.938G>T
  hgvsp: ENSP00000297504.6:p.Gly313Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.887G>T
  hgvsp: ENSP00000418271.1:p.Gly296Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*530G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.887G>T
  hgvsp: ENSP00000351717.4:p.Gly296Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.887G>T
  hgvsp: ENSP00000419558.1:p.Gly296Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*489G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.623G>T
  hgvsp: ENSP00000438776.1:p.Gly208Val
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.84G>T
  hgvsp: ENSP00000420162.1:p.Gly29Val
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly296Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

7-150732796-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732796
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732796
    reference: chr 7
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.945C>T
  hgvsp: ENST00000297504.6:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.894C>T
  hgvsp: ENST00000477092.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.894C>T
  hgvsp: ENST00000477719.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*537C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.630C>T
  hgvsp: ENST00000542328.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*461C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.91C>T
  hgvsp: ENST00000491920.1:c.91C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1005C>T
  hgvsp: ENST00000356058.4:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.894C>T
  hgvsp: ENST00000498578.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.894C>T
  hgvsp: ENST00000358849.4:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*496C>T
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly298Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

7-150732801-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732801
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732801
    reference: chr 7
allele count: 3
allele frequency: 2.478929102627665e-5
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*466G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.899G>A
  hgvsp: ENSP00000418271.1:p.Arg300Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.899G>A
  hgvsp: ENSP00000351717.4:p.Arg300Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*542G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1010G>A
  hgvsp: ENSP00000348353.4:p.Arg337Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.635G>A
  hgvsp: ENSP00000438776.1:p.Arg212Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*501G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.899G>A
  hgvsp: ENSP00000419891.1:p.Arg300Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.96G>A
  hgvsp: ENSP00000420162.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.950G>A
  hgvsp: ENSP00000297504.6:p.Arg317Gln
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.899G>A
  hgvsp: ENSP00000419558.1:p.Arg300Gln
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg300Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

7-150732801-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732801
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732801
    reference: chr 7
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.899G>T
  hgvsp: ENSP00000419558.1:p.Arg300Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*542G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.950G>T
  hgvsp: ENSP00000297504.6:p.Arg317Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*466G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1010G>T
  hgvsp: ENSP00000348353.4:p.Arg337Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.899G>T
  hgvsp: ENSP00000419891.1:p.Arg300Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.899G>T
  hgvsp: ENSP00000418271.1:p.Arg300Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.635G>T
  hgvsp: ENSP00000438776.1:p.Arg212Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.96G>T
  hgvsp: ENSP00000420162.1:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*501G>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.899G>T
  hgvsp: ENSP00000351717.4:p.Arg300Leu
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16836
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg300Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

7-150732809-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732809
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732809
    reference: chr 7
allele count: 16
allele frequency: 1.322073672555403e-4
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1018T>G
  hgvsp: ENSP00000348353.4:p.Ser340Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.907T>G
  hgvsp: ENSP00000418271.1:p.Ser303Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.907T>G
  hgvsp: ENSP00000351717.4:p.Ser303Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.643T>G
  hgvsp: ENSP00000438776.1:p.Ser215Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.104T>G
  hgvsp: ENSP00000420162.1:p.Ser36Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*474T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.907T>G
  hgvsp: ENSP00000419558.1:p.Ser303Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*550T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.907T>G
  hgvsp: ENSP00000419891.1:p.Ser303Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.958T>G
  hgvsp: ENSP00000297504.6:p.Ser320Ala
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*509T>G
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser303Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-150732812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732812
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732812
    reference: chr 7
allele count: 5163
allele frequency: 4.265320621912331e-2
allele num: 121046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.646C>T
  hgvsp: ENSP00000438776.1:p.Arg216Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.910C>T
  hgvsp: ENSP00000418271.1:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.107C>T
  hgvsp: ENSP00000420162.1:p.Arg37Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1021C>T
  hgvsp: ENSP00000348353.4:p.Arg341Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.910C>T
  hgvsp: ENSP00000419558.1:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*512C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*553C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.910C>T
  hgvsp: ENSP00000419891.1:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*477C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.910C>T
  hgvsp: ENSP00000351717.4:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.961C>T
  hgvsp: ENSP00000297504.6:p.Arg321Cys
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 344
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 8703
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 6.75e1
  variant carriers: 243
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 3.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 9.75e1
  variant carriers: 2342
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 4.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.75e1
  variant carriers: 292
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 6.25e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 3.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 7.25e1
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 5.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 4.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 8.25e1
  variant carriers: 324
genotype quality: GenotypeQuality
hgvs: p.Arg304Cys
num of homozygotes: 132
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

7-150732813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732813
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732813
    reference: chr 7
allele count: 4
allele frequency: 3.304911097891467e-5
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.108G>A
  hgvsp: ENSP00000420162.1:p.Arg37His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.911G>A
  hgvsp: ENSP00000419558.1:p.Arg304His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1022G>A
  hgvsp: ENSP00000348353.4:p.Arg341His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*513G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.647G>A
  hgvsp: ENSP00000438776.1:p.Arg216His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.911G>A
  hgvsp: ENSP00000351717.4:p.Arg304His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.911G>A
  hgvsp: ENSP00000418271.1:p.Arg304His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.962G>A
  hgvsp: ENSP00000297504.6:p.Arg321His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.911G>A
  hgvsp: ENSP00000419891.1:p.Arg304His
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*478G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*554G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg304His
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-150732828-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732828
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732828
    reference: chr 7
allele count: 3
allele frequency: 2.479215906649257e-5
allele num: 121006
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.926A>C
  hgvsp: ENSP00000351717.4:p.Gln309Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.123A>C
  hgvsp: ENSP00000420162.1:p.Gln42Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.977A>C
  hgvsp: ENSP00000297504.6:p.Gln326Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*528A>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1037A>C
  hgvsp: ENSP00000348353.4:p.Gln346Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*569A>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.926A>C
  hgvsp: ENSP00000419891.1:p.Gln309Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.662A>C
  hgvsp: ENSP00000438776.1:p.Gln221Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.926A>C
  hgvsp: ENSP00000418271.1:p.Gln309Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.926A>C
  hgvsp: ENSP00000419558.1:p.Gln309Pro
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*493A>C
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln309Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

7-150732831-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732831
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732831
    reference: chr 7
allele count: 1
allele frequency: 8.264462809917356e-6
allele num: 121000
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*531T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+2T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+2T>C
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
hgvs: c.927+2T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum

7-150732832-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732832
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732832
    reference: chr 7
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+3A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*532A>G
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.927+3A>G
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

7-150732834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732834
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732834
    reference: chr 7
allele count: 26
allele frequency: 2.148831366326159e-4
allele num: 120996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+5C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*534C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+5C>T
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.927+5C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

7-150732835-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732835
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732835
    reference: chr 7
allele count: 5
allele frequency: 4.132436319156322e-5
allele num: 120994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*535G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+6G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+6G>A
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.927+6G>A
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

7-150732837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732837
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732837
    reference: chr 7
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+8C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*537C>T
  variant of: http://identifiers.org/hgnc/49
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.927+8C>T
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

7-150732841-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732841
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732841
    reference: chr 7
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*541C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+12C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+12C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-150732849-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732849
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732849
    reference: chr 7
allele count: 52
allele frequency: 4.297662732652319e-4
allele num: 120996
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*549T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+20T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+20T>G
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8870
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

7-150732855-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732855
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732855
    reference: chr 7
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*555T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+26T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+26T>C
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-150732858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732858
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732858
    reference: chr 7
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*558C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+29C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+29C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

7-150732862-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732862
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732862
    reference: chr 7
allele count: 210
allele frequency: 1.736139817126606e-3
allele num: 120958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*562C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+33C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+33C>G
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 18028
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 6.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

7-150732862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732862
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732862
    reference: chr 7
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*562C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+33C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+33C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

7-150732865-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732865
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732865
    reference: chr 7
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*565C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+36C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+36C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

7-150732866-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732866
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732866
    reference: chr 7
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*566A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+37A>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+37A>G
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-150732870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732870
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732870
    reference: chr 7
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*570C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+41C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+41C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24624
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-150732871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732871
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732871
    reference: chr 7
allele count: 3
allele frequency: 2.481102271035612e-5
allele num: 120914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*571G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+42G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+42G>A
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

7-150732871-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732871
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732872
    reference: chr 7
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*574dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+45dupT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+45dupT
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18070
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

7-150732880-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732880
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732880
    reference: chr 7
allele count: 119
allele frequency: 9.842194064908856e-4
allele num: 120908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*580T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+51T>C
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+51T>C
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8794
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-150732882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732882
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732882
    reference: chr 7
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*582C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+53C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+53C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

7-150732884-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732884
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732884
    reference: chr 7
allele count: 8
allele frequency: 6.616929413905477e-5
allele num: 120902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*584C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+55C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+55C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8710
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24073
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

7-150732886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732886
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732886
    reference: chr 7
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+57C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+57C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

7-150732889-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732889
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732889
    reference: chr 7
allele count: 35
allele frequency: 2.895816785808843e-4
allele num: 120864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*589C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+60C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+60C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

7-150732890-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732890
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732890
    reference: chr 7
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*590G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+61G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+61G>A
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

7-150732894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732894
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732894
    reference: chr 7
allele count: 3
allele frequency: 2.48147167813658e-5
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*594C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+65C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+65C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

7-150732898-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732898
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732898
    reference: chr 7
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.124+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.927+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.927+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.927+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*570+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.927+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.978+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*494+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1038+69T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*598T>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.663+69T>G
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2633
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-150732907-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732907
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732907
    reference: chr 7
allele count: 12
allele frequency: 9.927857568336753e-5
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.979-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.125-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.664-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.928-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*495-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1039-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.928-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*571-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.928-62C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*607C>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.928-62C>A
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 8.25e1
  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: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

7-150732907-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732907
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732907
    reference: chr 7
allele count: 64
allele frequency: 5.294857369779601e-4
allele num: 120872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*607C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.125-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.928-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*495-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.979-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.928-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*571-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1039-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.664-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.928-62C>G
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.928-62C>G
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

7-150732911-CCTGGACTCCTTGTCCTGTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732911
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732890
    reference: chr 7
allele count: 14
allele frequency: 1.158154233053722e-4
allele num: 120882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 18000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18113
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: CCTGGACTCCTTGTCCTGTTTT
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

7-150732925-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732925
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732925
    reference: chr 7
allele count: 5
allele frequency: 4.135991397137894e-5
allele num: 120890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.928-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*625C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*495-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.125-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.928-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1039-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.928-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.979-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.928-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.664-44C>T
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*571-44C>T
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18006
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

7-150732928-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732928
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732927
    reference: chr 7
allele count: 1
allele frequency: 8.271572260455268e-6
allele num: 120896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.928-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*632delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.928-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.928-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1039-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.664-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.125-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.979-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*571-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.928-37delT
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*495-37delT
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: GT
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-150732932-TCTGGACTCCTTGTCCTGTTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732932
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732911
    reference: chr 7
allele count: 1
allele frequency: 8.270477702792114e-6
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24918
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: TCTGGACTCCTTGTCCTGTTTC
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

7-150732936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150732936
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150732936
    reference: chr 7
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000438776
  ensembl transcript: ENST00000542328
  gene symbol: ABCB8
  hgvsc: ENST00000542328.1:c.664-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420631
  ensembl transcript: ENST00000466514
  gene symbol: ABCB8
  hgvsc: ENST00000466514.1:c.*571-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000348353
  ensembl transcript: ENST00000356058
  gene symbol: ABCB8
  hgvsc: ENST00000356058.4:c.1039-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419891
  ensembl transcript: ENST00000477719
  gene symbol: ABCB8
  hgvsc: ENST00000477719.1:c.928-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000297504
  ensembl transcript: ENST00000297504
  gene symbol: ABCB8
  hgvsc: ENST00000297504.6:c.979-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420162
  ensembl transcript: ENST00000491920
  gene symbol: ABCB8
  hgvsc: ENST00000491920.1:c.125-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000418271
  ensembl transcript: ENST00000498578
  gene symbol: ABCB8
  hgvsc: ENST00000498578.1:c.928-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419558
  ensembl transcript: ENST00000477092
  gene symbol: ABCB8
  hgvsc: ENST00000477092.1:c.928-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000420216
  ensembl transcript: ENST00000470645
  gene symbol: ABCB8
  hgvsc: ENST00000470645.1:c.*636G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000419014
  ensembl transcript: ENST00000482309
  gene symbol: ABCB8
  hgvsc: ENST00000482309.1:c.*495-33G>A
  variant of: http://identifiers.org/hgnc/49
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197150
  ensembl protein: ENSP00000351717
  ensembl transcript: ENST00000358849
  gene symbol: ABCB8
  hgvsc: ENST00000358849.4:c.928-33G>A
  variant of: http://identifiers.org/hgnc/49
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 3589
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5349
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19418
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21449
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1957
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560549313358302e-5
allele num: 64080
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.424e0

MQRankSum
type: SiteQuality
SIO_000300: 3.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.35e-1

DP
type: SiteQuality
SIO_000300: 2.399567e6

MQ
type: SiteQuality
SIO_000300: 5.93e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.082e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.554e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19847
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3184
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5394
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21451
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1481
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.106458326861545e-5
allele num: 64382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.332089552238806e-4
allele num: 8576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 2.409525e6

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 3.247e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

GenotypeQuality
all individuals: 1977
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21461
bin: 9.75e1
variant carriers: 252

GenotypeQuality
all individuals: 3078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5453
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.807767752059631e-5
allele num: 10196
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 230
allele frequency: 3.563350168871812e-3
allele num: 64546
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.693491306354824e-5
allele num: 12998
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 18
allele frequency: 2.723146747352496e-3
allele num: 6610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 5.52e0

DP
type: SiteQuality
SIO_000300: 2.417963e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 20814
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2654
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21276
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.956564273136372e-4
allele num: 10222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13638
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

FS
type: SiteQuality
SIO_000300: 4.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.608e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.831e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

DP
type: SiteQuality
SIO_000300: 2.401771e6

GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21819
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2266
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65534
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.515e0

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

DP
type: SiteQuality
SIO_000300: 2.428052e6

MQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.602e0

FS
type: SiteQuality
SIO_000300: 3.444e0

QD
type: SiteQuality
SIO_000300: 1.299e1

GenotypeDepth
all individuals: 16190
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1732
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5841
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22630
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21275
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036652394400413e-5
allele num: 65862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15780
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQ
type: SiteQuality
SIO_000300: 5.281e1

DP
type: SiteQuality
SIO_000300: 2.440602e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.044e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
SIO_000300: 6.52e0

GenotypeDepth
all individuals: 1599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5933
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21279
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-5
allele num: 66060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.182762458266353e-5
allele num: 16174
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.450797e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.923e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.461e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

FS
type: SiteQuality
SIO_000300: 6.850000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-1

GenotypeDepth
all individuals: 1945
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23168
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21281
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51290508033526e-5
allele num: 66098
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-1

FS
type: SiteQuality
SIO_000300: 3.341e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 2.452222e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

QD
type: SiteQuality
SIO_000300: 1.377e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

GenotypeDepth
all individuals: 1094
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23168
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21281
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.139489194499017e-5
allele num: 16288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.377e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

FS
type: SiteQuality
SIO_000300: 3.341e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

DP
type: SiteQuality
SIO_000300: 2.452222e6

GenotypeDepth
all individuals: 7736
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21279
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025810160670519e-5
allele num: 66098
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.73e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 2.45229e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.526e1

FS
type: SiteQuality
SIO_000300: 4.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e0

GenotypeDepth
all individuals: 3200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21283
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2197
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.222045704509349e-4
allele num: 16366
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.713e0

DP
type: SiteQuality
SIO_000300: 2.45428e6

FS
type: SiteQuality
SIO_000300: 4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.399e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeDepth
all individuals: 16594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21287
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.099048548426445e-5
allele num: 16396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5355587808418e-5
allele num: 66144
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.674922600619196e-5
allele num: 10336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.28e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 2.454948e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeDepth
all individuals: 3845
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1526
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23162
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511852926947267e-5
allele num: 66144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

DP
type: SiteQuality
SIO_000300: 2.454948e6

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

GenotypeDepth
all individuals: 2040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21298
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.078288353999514e-5
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.551045064636945e-5
allele num: 66216
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.52e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.96e0

DP
type: SiteQuality
SIO_000300: 2.457134e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.51e-1

QD
type: SiteQuality
SIO_000300: 1.606e1

GenotypeDepth
all individuals: 1936
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23287
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21297
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.856136943061794e-4
allele num: 16474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.543e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

DP
type: SiteQuality
SIO_000300: 2.457565e6

FS
type: SiteQuality
SIO_000300: 1.101e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-2

GenotypeDepth
all individuals: 1936
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21297
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66248
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.035085589413621e-4
allele num: 16474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

QD
type: SiteQuality
SIO_000300: 1.543e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.101e0

DP
type: SiteQuality
SIO_000300: 2.457565e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

GenotypeDepth
all individuals: 2697
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21290
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 23325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016409266409266e-5
allele num: 66304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.004e0

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.458252e6

FS
type: SiteQuality
SIO_000300: 1.844e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

GenotypeDepth
all individuals: 3200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6059
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507340749449821e-5
allele num: 66342
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.281000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.745e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: -5.951e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 2.45885e6

QD
type: SiteQuality
SIO_000300: 1.491e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeDepth
all individuals: 3600
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1815
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23382
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6063
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21292
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.458886e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.6017e1

QD
type: SiteQuality
SIO_000300: 1.307e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.151e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeDepth
all individuals: 221
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6062
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23381
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 321
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.043e0

VQSLOD
type: SiteQuality
SIO_000300: -1.026e-1

FS
type: SiteQuality
SIO_000300: 1.694e0

DP
type: SiteQuality
SIO_000300: 2.458878e6

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.003e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23344
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1554
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.364e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.134e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 2.458739e6

FS
type: SiteQuality
SIO_000300: 5.421e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.036e0

MQ
type: SiteQuality
SIO_000300: 5.926e1

GenotypeDepth
all individuals: 3199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23332
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21289
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6073
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 2.458974e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.04e0

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 4.483e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.86e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-1

GenotypeDepth
all individuals: 2697
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 310
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.45908e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.33e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.841e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeDepth
all individuals: 1093
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2243
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66416
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 2.45964e6

MQRankSum
type: SiteQuality
SIO_000300: -6.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.128e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.262e0

QD
type: SiteQuality
SIO_000300: 1.368e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 16795
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6097
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1821
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21285
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010597302504817e-5
allele num: 66432
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.202e0

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

FS
type: SiteQuality
SIO_000300: 1.843e0

DP
type: SiteQuality
SIO_000300: 2.460062e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21285
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.256e0

QD
type: SiteQuality
SIO_000300: 1.247e1

VQSLOD
type: SiteQuality
SIO_000300: 8.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.142e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

DP
type: SiteQuality
SIO_000300: 2.460043e6

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2696
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21285
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23490
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQ
type: SiteQuality
SIO_000300: 5.902e1

VQSLOD
type: SiteQuality
SIO_000300: -3.466e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 2.460088e6

FS
type: SiteQuality
SIO_000300: 3.589e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.61e-1

QD
type: SiteQuality
SIO_000300: 1.216e1

GenotypeDepth
all individuals: 1598
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21284
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504664459825459e-5
allele num: 66460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.079e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.460318e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e-1

QD
type: SiteQuality
SIO_000300: 3.06e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeDepth
all individuals: 1933
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21284
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 2.460371e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.674e0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeDepth
all individuals: 3597
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21284
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23547
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009872381411028e-5
allele num: 66448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.274287039183863e-4
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.674e0

DP
type: SiteQuality
SIO_000300: 2.460371e6

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeDepth
all individuals: 3714
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1558
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.459892e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.141e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

GenotypeDepth
all individuals: 733
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21274
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6074
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010325416177489e-5
allele num: 66438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.98e-1

DP
type: SiteQuality
SIO_000300: 2.460045e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 3.223e0

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeDepth
all individuals: 1093
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.223e0

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.98e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 2.460045e6

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeDepth
all individuals: 518
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6068
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21277
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 1557
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.408405334617816e-4
allele num: 66434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.255e1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

FS
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.459669e6

VQSLOD
type: SiteQuality
SIO_000300: 2.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e-1

GenotypeDepth
all individuals: 2670
bin: 5.75e1
variant carriers: 165

GenotypeQuality
all individuals: 1497
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 7.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1765
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23168
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2364
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5965
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1139
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 22106
bin: 9.75e1
variant carriers: 5017

GenotypeQuality
all individuals: 235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3956
allele frequency: 5.952810882388347e-2
allele num: 66456
num of homozygotes: 111

Latino
type: Population
allele count: 274
allele frequency: 2.367375151200968e-2
allele num: 11574
num of homozygotes: 4

South Asian
type: Population
allele count: 332
allele frequency: 2.010902483343428e-2
allele num: 16510
num of homozygotes: 7

Other
type: Population
allele count: 26
allele frequency: 2.876106194690265e-2
allele num: 904
num of homozygotes: 1

African
type: Population
allele count: 149
allele frequency: 1.438779451525686e-2
allele num: 10356
num of homozygotes: 0

East Asian
type: Population
allele count: 188
allele frequency: 2.177942539388323e-2
allele num: 8632
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 238
allele frequency: 3.598427577865135e-2
allele num: 6614
num of homozygotes: 6

DP
type: SiteQuality
SIO_000300: 2.537978e6

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.259e1

GenotypeDepth
all individuals: 1951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18463
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 6650
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2701
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

QD
type: SiteQuality
SIO_000300: 1.106e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 9.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 2.255061e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

GenotypeDepth
all individuals: 4290
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8782
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 252
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2698
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18460
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6636
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.517391959042313e-5
allele num: 66410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.258e0

VQSLOD
type: SiteQuality
SIO_000300: -1.072e0

QD
type: SiteQuality
SIO_000300: 7.86e0

FS
type: SiteQuality
SIO_000300: 1.283e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.394e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.253421e6

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18458
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24723
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505842669557885e-5
allele num: 66408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.58e-1

DP
type: SiteQuality
SIO_000300: 2.253088e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.192e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

FS
type: SiteQuality
SIO_000300: 1.3012e1

MQ
type: SiteQuality
SIO_000300: 5.876e1

QD
type: SiteQuality
SIO_000300: 8.35e0

MQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

GenotypeDepth
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24737
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18459
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.233e0

QD
type: SiteQuality
SIO_000300: 1.265e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

DP
type: SiteQuality
SIO_000300: 2.25301e6

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 1.0352e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 3321
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1386
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18463
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6629
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.10824323103334e-4
allele num: 66406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.061981077428075e-3
allele num: 10358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 2.253322e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

VQSLOD
type: SiteQuality
SIO_000300: 5.39e0

QD
type: SiteQuality
SIO_000300: 1.268e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeDepth
all individuals: 2698
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 384
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24697
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18440
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6625
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2685
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.827186715582159e-4
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.251572e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 2.307e1

MQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

FS
type: SiteQuality
SIO_000300: 1.227e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.174e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeDepth
all individuals: 1386
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2698
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18433
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2682
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.982e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.074e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 8.56e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 2.251132e6

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.087e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2686
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18432
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505661286437003e-5
allele num: 66416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.250929e6

VQSLOD
type: SiteQuality
SIO_000300: -1.975e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

FS
type: SiteQuality
SIO_000300: 1.4299e1

QD
type: SiteQuality
SIO_000300: 1.232e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.774e0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18438
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 2002
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 50
allele frequency: 7.528986598403855e-4
allele num: 66410
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.353e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.250823e6

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.47e-1

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18400
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2680
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.473e0

DP
type: SiteQuality
SIO_000300: 2.248155e6

FS
type: SiteQuality
SIO_000300: 5.034e0

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.251e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

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

GenotypeQuality
all individuals: 2001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24619
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18392
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.247547e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.309e0

QD
type: SiteQuality
SIO_000300: 1.062e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.255e0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2440
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24563
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18452
bin: 9.75e1
variant carriers: 209

GenotypeQuality
all individuals: 1991
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 197
allele frequency: 1.904117533346221e-2
allele num: 10346
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.518888955835392e-5
allele num: 66388
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.640055296353896e-4
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

DP
type: SiteQuality
SIO_000300: 2.249441e6

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24563
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18452
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506296318611797e-5
allele num: 66388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.322e1

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.249441e6

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2676
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2000
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24597
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506341698550899e-5
allele num: 66386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.403e0

VQSLOD
type: SiteQuality
SIO_000300: -1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

MQ
type: SiteQuality
SIO_000300: 5.888e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 8.82e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.909e0

DP
type: SiteQuality
SIO_000300: 2.241424e6

GenotypeQuality
all individuals: 2449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24611
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.281000000000001e0

DP
type: SiteQuality
SIO_000300: 2.241554e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.73e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.558e0

VQSLOD
type: SiteQuality
SIO_000300: -9.761e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

GenotypeQuality
all individuals: 18271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2448
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6618
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506750241080039e-5
allele num: 66368
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 2.240949e6

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18272
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.901353965183752e-4
allele num: 10340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

DP
type: SiteQuality
SIO_000300: 2.240672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.654e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

GenotypeQuality
all individuals: 411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18272
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506931886678722e-5
allele num: 66360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.912e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

DP
type: SiteQuality
SIO_000300: 2.240672e6

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.654e0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18276
bin: 9.75e1
variant carriers: 119

GenotypeQuality
all individuals: 1244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24367
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2667
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.296904720733183e-3
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.552352048558422e-4
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 91
allele frequency: 1.371142719382835e-3
allele num: 66368
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.768516727905628e-4
allele num: 10342
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

QD
type: SiteQuality
SIO_000300: 1.448e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

DP
type: SiteQuality
SIO_000300: 2.237518e6

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

GenotypeQuality
all individuals: 2439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6601
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18181
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.606e0

MQRankSum
type: SiteQuality
SIO_000300: -1.007e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 2.233026e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.7462e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.488e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.609e0

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

GenotypeQuality
all individuals: 1657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18180
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 206
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.736943907156673e-4
allele num: 10340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.828e0

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.347e1

DP
type: SiteQuality
SIO_000300: 2.230881e6

GenotypeQuality
all individuals: 454
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1658
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18173
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24243
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.873e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.364e0

FS
type: SiteQuality
SIO_000300: 3.007e0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.177e1

DP
type: SiteQuality
SIO_000300: 2.230379e6

VQSLOD
type: SiteQuality
SIO_000300: -1.408e0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18179
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 24293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50779530170984e-5
allele num: 66322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.804953560371517e-4
allele num: 10336
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.916825177243646e-4
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.151096570943899e-3
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.229796e6

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 5.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.498e1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24466
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66312
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.228356e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24478
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18132
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 465
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.52134072823728e-5
allele num: 66352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 5.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.88e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.39e0

DP
type: SiteQuality
SIO_000300: 2.226002e6

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18124
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1968
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24580
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 2.225273e6

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

FS
type: SiteQuality
SIO_000300: 7.215e0

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

GenotypeQuality
all individuals: 440
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18163
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.029362997799283e-5
allele num: 66342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.240368306275745e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.72e-1

FS
type: SiteQuality
SIO_000300: 1.741e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

DP
type: SiteQuality
SIO_000300: 2.225321e6

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18163
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 228
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 63
allele frequency: 9.49624672153387e-4
allele num: 66342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 1.741e0

QD
type: SiteQuality
SIO_000300: 1.323e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

DP
type: SiteQuality
SIO_000300: 2.225321e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.72e-1

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 245
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2611
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.158480074142725e-3
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.521613311629589e-5
allele num: 66348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.81e0

DP
type: SiteQuality
SIO_000300: 2.221739e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -7.497e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.662e1

FS
type: SiteQuality
SIO_000300: 1.142e0

QD
type: SiteQuality
SIO_000300: 2.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18095
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6372
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.025911419102139e-5
allele num: 66380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.741e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.233e0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 2.220759e6

QD
type: SiteQuality
SIO_000300: 1.342e1

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.517e0

GenotypeQuality
all individuals: 1222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6370
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24979
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.221042e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

MQ
type: SiteQuality
SIO_000300: 6.042e1

MQRankSum
type: SiteQuality
SIO_000300: -7.54e-1

QD
type: SiteQuality
SIO_000300: 1.271e1

FS
type: SiteQuality
SIO_000300: 4.013e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.342e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.23e-1

GenotypeQuality
all individuals: 185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18098
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.824e1

FS
type: SiteQuality
SIO_000300: 8.151e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

QD
type: SiteQuality
SIO_000300: 2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: -1.183e0

DP
type: SiteQuality
SIO_000300: 2.220883e6

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1954
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0