6-157528147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528147
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5818G>A
  hgvsp: ENSP00000275248.4:p.Val1940Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4399G>A
  hgvsp: ENSP00000412835.2:p.Val1467Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.5992G>A
  hgvsp: ENSP00000356116.1:p.Val1998Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5833G>A
  hgvsp: ENSP00000055163.7:p.Val1945Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5872G>A
  hgvsp: ENSP00000344546.4:p.Val1958Met
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43734
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val1958Met
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-157528160-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528160
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528160
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5831A>G
  hgvsp: ENSP00000275248.4:p.Asp1944Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5846A>G
  hgvsp: ENSP00000055163.7:p.Asp1949Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5885A>G
  hgvsp: ENSP00000344546.4:p.Asp1962Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6005A>G
  hgvsp: ENSP00000356116.1:p.Asp2002Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4412A>G
  hgvsp: ENSP00000412835.2:p.Asp1471Gly
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp1962Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

6-157528164-C-CAGTAAGTTCGACAAGCTGCCAATAAAGATAGTCAAAAAGAACAACCTGTTTGTTGTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528164
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528221
    reference: chr 6
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: CAGTAAGTTCGACAAGCTGCCAATAAAGATAGTCAAAAAGAACAACCTGTTTGTTGTT
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43735
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-157528164-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528164
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528164
    reference: chr 6
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5835C>G
  hgvsp: ENST00000275248.4:c.5835C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4416C>G
  hgvsp: ENST00000414678.2:c.4416C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5850C>G
  hgvsp: ENST00000350026.5:c.5850C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6009C>G
  hgvsp: ENST00000367148.1:c.6009C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5889C>G
  hgvsp: ENST00000346085.5:c.5889C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala1963Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-157528173-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528173
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528173
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5844C>A
  hgvsp: ENST00000275248.4:c.5844C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5859C>A
  hgvsp: ENST00000350026.5:c.5859C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4425C>A
  hgvsp: ENST00000414678.2:c.4425C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6018C>A
  hgvsp: ENST00000367148.1:c.6018C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5898C>A
  hgvsp: ENST00000346085.5:c.5898C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser1966Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

6-157528175-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528175
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528175
    reference: chr 6
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5846A>G
  hgvsp: ENSP00000275248.4:p.Lys1949Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5900A>G
  hgvsp: ENSP00000344546.4:p.Lys1967Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4427A>G
  hgvsp: ENSP00000412835.2:p.Lys1476Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5861A>G
  hgvsp: ENSP00000055163.7:p.Lys1954Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6020A>G
  hgvsp: ENSP00000356116.1:p.Lys2007Arg
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43736
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9475
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys1967Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-157528196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528196
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528196
    reference: chr 6
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4448T>C
  hgvsp: ENSP00000412835.2:p.Ile1483Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5882T>C
  hgvsp: ENSP00000055163.7:p.Ile1961Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6041T>C
  hgvsp: ENSP00000356116.1:p.Ile2014Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5867T>C
  hgvsp: ENSP00000275248.4:p.Ile1956Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5921T>C
  hgvsp: ENSP00000344546.4:p.Ile1974Thr
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43735
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile1974Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

6-157528197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528197
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528197
    reference: chr 6
allele count: 1221
allele frequency: 1.005848916714721e-2
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5868C>T
  hgvsp: ENST00000275248.4:c.5868C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6042C>T
  hgvsp: ENST00000367148.1:c.6042C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5922C>T
  hgvsp: ENST00000346085.5:c.5922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5883C>T
  hgvsp: ENST00000350026.5:c.5883C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4449C>T
  hgvsp: ENST00000414678.2:c.4449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 9.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 8.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 9.75e1
  variant carriers: 1063
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 7.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile1974Ile
num of homozygotes: 13
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

6-157528202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528202
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528202
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5888G>A
  hgvsp: ENSP00000055163.7:p.Gly1963Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4454G>A
  hgvsp: ENSP00000412835.2:p.Gly1485Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5873G>A
  hgvsp: ENSP00000275248.4:p.Gly1958Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6047G>A
  hgvsp: ENSP00000356116.1:p.Gly2016Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5927G>A
  hgvsp: ENSP00000344546.4:p.Gly1976Glu
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43804
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9522
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly1976Glu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

6-157528203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528203
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528203
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5874G>A
  hgvsp: ENST00000275248.4:c.5874G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6048G>A
  hgvsp: ENST00000367148.1:c.6048G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5889G>A
  hgvsp: ENST00000350026.5:c.5889G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4455G>A
  hgvsp: ENST00000414678.2:c.4455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5928G>A
  hgvsp: ENST00000346085.5:c.5928G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly1976Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-32505295-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505295
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505295
    reference: chr 8
allele count: 2
allele frequency: 1.682991686021071e-5
allele num: 118836
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42094C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.59C>G
  hgvsp: ENSP00000433289.1:p.Ser20Cys
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42094C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33213C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30892C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42094C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30892C>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser20Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

6-157528209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528209
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528209
    reference: chr 6
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5895G>A
  hgvsp: ENST00000350026.5:c.5895G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4461G>A
  hgvsp: ENST00000414678.2:c.4461G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5880G>A
  hgvsp: ENST00000275248.4:c.5880G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6054G>A
  hgvsp: ENST00000367148.1:c.6054G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5934G>A
  hgvsp: ENST00000346085.5:c.5934G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu1978Leu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

6-157528212-TCTTCTTCACC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528212
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528202
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsp: ENSP00000356116.1:p.Leu2020ThrfsTer38
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsp: ENSP00000055163.7:p.Leu1967ThrfsTer38
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsp: ENSP00000344546.4:p.Leu1980ThrfsTer38
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsp: ENSP00000412835.2:p.Leu1489ThrfsTer38
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsp: ENSP00000275248.4:p.Leu1962ThrfsTer38
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9542
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43803
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu1980ThrfsTer38
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: TCTTCTTCACC
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

6-157528219-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528219
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528219
    reference: chr 6
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4471C>T
  hgvsp: ENSP00000412835.2:p.His1491Tyr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5890C>T
  hgvsp: ENSP00000275248.4:p.His1964Tyr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6064C>T
  hgvsp: ENSP00000356116.1:p.His2022Tyr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5905C>T
  hgvsp: ENSP00000055163.7:p.His1969Tyr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5944C>T
  hgvsp: ENSP00000344546.4:p.His1982Tyr
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His1982Tyr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

6-157528221-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528221
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528221
    reference: chr 6
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5907C>T
  hgvsp: ENST00000350026.5:c.5907C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6066C>T
  hgvsp: ENST00000367148.1:c.6066C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5946C>T
  hgvsp: ENST00000346085.5:c.5946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5892C>T
  hgvsp: ENST00000275248.4:c.5892C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4473C>T
  hgvsp: ENST00000414678.2:c.4473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43803
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His1982His
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-157528224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528224
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528224
    reference: chr 6
allele count: 28
allele frequency: 2.306615042425241e-4
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5910C>T
  hgvsp: ENST00000350026.5:c.5910C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6069C>T
  hgvsp: ENST00000367148.1:c.6069C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5949C>T
  hgvsp: ENST00000346085.5:c.5949C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5895C>T
  hgvsp: ENST00000275248.4:c.5895C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4476C>T
  hgvsp: ENST00000414678.2:c.4476C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9531
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43808
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His1983His
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

6-157528225-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528225
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528226
    reference: chr 6
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5911_5912insC
  hgvsp: ENSP00000055163.7:p.Glu1971AlafsTer13
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4477_4478insC
  hgvsp: ENSP00000412835.2:p.Glu1493AlafsTer13
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5950_5951insC
  hgvsp: ENSP00000344546.4:p.Glu1984AlafsTer13
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6070_6071insC
  hgvsp: ENSP00000356116.1:p.Glu2024AlafsTer13
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5896_5897insC
  hgvsp: ENSP00000275248.4:p.Glu1966AlafsTer13
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43804
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu1984AlafsTer13
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

6-157528229-ATCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528229
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528226
    reference: chr 6
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5955_5957delTCC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4482_4484delTCC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5916_5918delTCC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5901_5903delTCC
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6075_6077delTCC
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His1985_Pro1986delinsGln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: ATCC
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

6-157528234-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528234
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528233
    reference: chr 6
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5960delA
  hgvsp: ENSP00000344546.4:p.Glu1987GlyfsTer34
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4487delA
  hgvsp: ENSP00000412835.2:p.Glu1496GlyfsTer34
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5921delA
  hgvsp: ENSP00000055163.7:p.Glu1974GlyfsTer34
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6080delA
  hgvsp: ENSP00000356116.1:p.Glu2027GlyfsTer34
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5906delA
  hgvsp: ENSP00000275248.4:p.Glu1969GlyfsTer34
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1987GlyfsTer34
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: GA
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-157528237-A-AAGGAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528237
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528242
    reference: chr 6
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: AAGGAT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5923_5924insAGGAT
  hgvsp: ENSP00000055163.7:p.Arg1975LysfsTer35
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5908_5909insAGGAT
  hgvsp: ENSP00000275248.4:p.Arg1970LysfsTer35
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4489_4490insAGGAT
  hgvsp: ENSP00000412835.2:p.Arg1497LysfsTer35
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6082_6083insAGGAT
  hgvsp: ENSP00000356116.1:p.Arg2028LysfsTer35
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5962_5963insAGGAT
  hgvsp: ENSP00000344546.4:p.Arg1988LysfsTer35
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1988LysfsTer35
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-157528240-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528240
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528240
    reference: chr 6
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6085A>C
  hgvsp: ENSP00000356116.1:p.Lys2029Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5965A>C
  hgvsp: ENSP00000344546.4:p.Lys1989Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4492A>C
  hgvsp: ENSP00000412835.2:p.Lys1498Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5926A>C
  hgvsp: ENSP00000055163.7:p.Lys1976Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5911A>C
  hgvsp: ENSP00000275248.4:p.Lys1971Gln
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys1989Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/6-157528241-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528241
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528241
    reference: chr 6
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4493A>C
  hgvsp: ENSP00000412835.2:p.Lys1498Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5927A>C
  hgvsp: ENSP00000055163.7:p.Lys1976Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5966A>C
  hgvsp: ENSP00000344546.4:p.Lys1989Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5912A>C
  hgvsp: ENSP00000275248.4:p.Lys1971Thr
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6086A>C
  hgvsp: ENSP00000356116.1:p.Lys2029Thr
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys1989Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum

6-157528243-CGAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528243
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528240
    reference: chr 6
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6089_6091delGAG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4496_4498delGAG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5930_5932delGAG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5915_5917delGAG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5969_5971delGAG
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9558
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1990_Ala1991delinsPro
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: CGAG
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

6-157528244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528244
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528244
    reference: chr 6
allele count: 5
allele frequency: 4.118616144975288e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6089G>A
  hgvsp: ENSP00000356116.1:p.Arg2030Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4496G>A
  hgvsp: ENSP00000412835.2:p.Arg1499Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5930G>A
  hgvsp: ENSP00000055163.7:p.Arg1977Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5969G>A
  hgvsp: ENSP00000344546.4:p.Arg1990Gln
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5915G>A
  hgvsp: ENSP00000275248.4:p.Arg1972Gln
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg1990Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

6-157528247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528247
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528247
    reference: chr 6
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5918C>T
  hgvsp: ENSP00000275248.4:p.Ala1973Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5933C>T
  hgvsp: ENSP00000055163.7:p.Ala1978Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5972C>T
  hgvsp: ENSP00000344546.4:p.Ala1991Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4499C>T
  hgvsp: ENSP00000412835.2:p.Ala1500Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6092C>T
  hgvsp: ENSP00000356116.1:p.Ala2031Val
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala1991Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

6-157528248-A-AGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528248
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528250
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: AGT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5973_5974insGT
  hgvsp: ENSP00000344546.4:p.Pro1992ValfsTer30
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6093_6094insGT
  hgvsp: ENSP00000356116.1:p.Pro2032ValfsTer30
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5934_5935insGT
  hgvsp: ENSP00000055163.7:p.Pro1979ValfsTer30
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4500_4501insGT
  hgvsp: ENSP00000412835.2:p.Pro1501ValfsTer30
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5919_5920insGT
  hgvsp: ENSP00000275248.4:p.Pro1974ValfsTer30
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9568
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1992ValfsTer30
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

6-157528248-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528248
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528248
    reference: chr 6
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4500A>T
  hgvsp: ENST00000414678.2:c.4500A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6093A>T
  hgvsp: ENST00000367148.1:c.6093A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5973A>T
  hgvsp: ENST00000346085.5:c.5973A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5934A>T
  hgvsp: ENST00000350026.5:c.5934A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5919A>T
  hgvsp: ENST00000275248.4:c.5919A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9568
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala1991Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

6-157528250-C-CTTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528250
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528253
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: CTTG
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4502_4503insTTG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5936_5937insTTG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5975_5976insTTG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6095_6096insTTG
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5921_5922insTTG
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro1992_Gln1993insTrp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

6-157528250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528250
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528250
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6095C>T
  hgvsp: ENSP00000356116.1:p.Pro2032Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5975C>T
  hgvsp: ENSP00000344546.4:p.Pro1992Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4502C>T
  hgvsp: ENSP00000412835.2:p.Pro1501Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5936C>T
  hgvsp: ENSP00000055163.7:p.Pro1979Leu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5921C>T
  hgvsp: ENSP00000275248.4:p.Pro1974Leu
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1992Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-157528251-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528251
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528251
    reference: chr 6
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5976G>A
  hgvsp: ENST00000346085.5:c.5976G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4503G>A
  hgvsp: ENST00000414678.2:c.4503G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6096G>A
  hgvsp: ENST00000367148.1:c.6096G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5922G>A
  hgvsp: ENST00000275248.4:c.5922G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5937G>A
  hgvsp: ENST00000350026.5:c.5937G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro1992Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-157528256-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528256
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528256
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4508C>G
  hgvsp: ENSP00000412835.2:p.Thr1503Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5981C>G
  hgvsp: ENSP00000344546.4:p.Thr1994Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5942C>G
  hgvsp: ENSP00000055163.7:p.Thr1981Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6101C>G
  hgvsp: ENSP00000356116.1:p.Thr2034Ser
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5927C>G
  hgvsp: ENSP00000275248.4:p.Thr1976Ser
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9578
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43807
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr1994Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

6-157528256-C-CGATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528256
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528260
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: CGATT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5981_5982insGATT
  hgvsp: ENSP00000344546.4:p.Tyr1995IlefsTer3
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5927_5928insGATT
  hgvsp: ENSP00000275248.4:p.Tyr1977IlefsTer3
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6101_6102insGATT
  hgvsp: ENSP00000356116.1:p.Tyr2035IlefsTer3
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5942_5943insGATT
  hgvsp: ENSP00000055163.7:p.Tyr1982IlefsTer3
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4508_4509insGATT
  hgvsp: ENSP00000412835.2:p.Tyr1504IlefsTer3
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9578
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr1995IlefsTer3
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

6-157528257-CTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528257
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528255
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6104_6105delAT
  hgvsp: ENSP00000356116.1:p.Tyr2035Ter
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4511_4512delAT
  hgvsp: ENSP00000412835.2:p.Tyr1504Ter
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5984_5985delAT
  hgvsp: ENSP00000344546.4:p.Tyr1995Ter
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5945_5946delAT
  hgvsp: ENSP00000055163.7:p.Tyr1982Ter
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5930_5931delAT
  hgvsp: ENSP00000275248.4:p.Tyr1977Ter
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr1995Ter
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: CTA
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-157528262-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528262
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528262
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5948A>G
  hgvsp: ENSP00000055163.7:p.Glu1983Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5987A>G
  hgvsp: ENSP00000344546.4:p.Glu1996Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5933A>G
  hgvsp: ENSP00000275248.4:p.Glu1978Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4514A>G
  hgvsp: ENSP00000412835.2:p.Glu1505Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6107A>G
  hgvsp: ENSP00000356116.1:p.Glu2036Gly
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1996Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

6-157528266-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528266
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528266
    reference: chr 6
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6111A>G
  hgvsp: ENST00000367148.1:c.6111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5937A>G
  hgvsp: ENST00000275248.4:c.5937A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5991A>G
  hgvsp: ENST00000346085.5:c.5991A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4518A>G
  hgvsp: ENST00000414678.2:c.4518A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5952A>G
  hgvsp: ENST00000350026.5:c.5952A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9587
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys1997Lys
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: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-157528274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528274
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528274
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6119A>G
  hgvsp: ENSP00000356116.1:p.Asp2040Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5960A>G
  hgvsp: ENSP00000055163.7:p.Asp1987Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4526A>G
  hgvsp: ENSP00000412835.2:p.Asp1509Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5945A>G
  hgvsp: ENSP00000275248.4:p.Asp1982Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.5999A>G
  hgvsp: ENSP00000344546.4:p.Asp2000Gly
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp2000Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-157528278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528278
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528278
    reference: chr 6
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4530G>A
  hgvsp: ENST00000414678.2:c.4530G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6123G>A
  hgvsp: ENST00000367148.1:c.6123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6003G>A
  hgvsp: ENST00000346085.5:c.6003G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5949G>A
  hgvsp: ENST00000275248.4:c.5949G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5964G>A
  hgvsp: ENST00000350026.5:c.5964G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9591
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu2001Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-157528280-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528280
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528280
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5951A>G
  hgvsp: ENSP00000275248.4:p.Asp1984Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6005A>G
  hgvsp: ENSP00000344546.4:p.Asp2002Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4532A>G
  hgvsp: ENSP00000412835.2:p.Asp1511Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6125A>G
  hgvsp: ENSP00000356116.1:p.Asp2042Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5966A>G
  hgvsp: ENSP00000055163.7:p.Asp1989Gly
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp2002Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

6-157528282-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528282
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528282
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4534A>G
  hgvsp: ENSP00000412835.2:p.Lys1512Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6127A>G
  hgvsp: ENSP00000356116.1:p.Lys2043Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6007A>G
  hgvsp: ENSP00000344546.4:p.Lys2003Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5953A>G
  hgvsp: ENSP00000275248.4:p.Lys1985Glu
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5968A>G
  hgvsp: ENSP00000055163.7:p.Lys1990Glu
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9593
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys2003Glu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-157528283-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528283
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528282
    reference: chr 6
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4540delG
  hgvsp: ENSP00000412835.2:p.Val1514TrpfsTer16
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5959delG
  hgvsp: ENSP00000275248.4:p.Val1987TrpfsTer16
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5974delG
  hgvsp: ENSP00000055163.7:p.Val1992TrpfsTer16
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6133delG
  hgvsp: ENSP00000356116.1:p.Val2045TrpfsTer16
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6013delG
  hgvsp: ENSP00000344546.4:p.Val2005TrpfsTer16
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43808
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val2005TrpfsTer16
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: AG
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-157528284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528284
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528284
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6129G>A
  hgvsp: ENST00000367148.1:c.6129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5970G>A
  hgvsp: ENST00000350026.5:c.5970G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6009G>A
  hgvsp: ENST00000346085.5:c.6009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4536G>A
  hgvsp: ENST00000414678.2:c.4536G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5955G>A
  hgvsp: ENST00000275248.4:c.5955G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys2003Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-157528292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528292
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528292
    reference: chr 6
allele count: 11
allele frequency: 9.060507717905211e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6137C>T
  hgvsp: ENSP00000356116.1:p.Ala2046Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5978C>T
  hgvsp: ENSP00000055163.7:p.Ala1993Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5963C>T
  hgvsp: ENSP00000275248.4:p.Ala1988Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4544C>T
  hgvsp: ENSP00000412835.2:p.Ala1515Val
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6017C>T
  hgvsp: ENSP00000344546.4:p.Ala2006Val
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9587
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala2006Val
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

6-157528294-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528294
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528294
    reference: chr 6
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5965T>C
  hgvsp: ENSP00000275248.4:p.Cys1989Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4546T>C
  hgvsp: ENSP00000412835.2:p.Cys1516Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.5980T>C
  hgvsp: ENSP00000055163.7:p.Cys1994Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6139T>C
  hgvsp: ENSP00000356116.1:p.Cys2047Arg
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6019T>C
  hgvsp: ENSP00000344546.4:p.Cys2007Arg
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys2007Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-157528326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528326
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528326
    reference: chr 6
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6051C>T
  hgvsp: ENST00000346085.5:c.6051C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5997C>T
  hgvsp: ENST00000275248.4:c.5997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6171C>T
  hgvsp: ENST00000367148.1:c.6171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6012C>T
  hgvsp: ENST00000350026.5:c.6012C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4578C>T
  hgvsp: ENST00000414678.2:c.4578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43803
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu2017Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

6-157528327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528327
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528327
    reference: chr 6
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6052G>A
  hgvsp: ENSP00000344546.4:p.Glu2018Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6013G>A
  hgvsp: ENSP00000055163.7:p.Glu2005Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4579G>A
  hgvsp: ENSP00000412835.2:p.Glu1527Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.5998G>A
  hgvsp: ENSP00000275248.4:p.Glu2000Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6172G>A
  hgvsp: ENSP00000356116.1:p.Glu2058Lys
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43803
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu2018Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-157528329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528329
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528329
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6000G>A
  hgvsp: ENST00000275248.4:c.6000G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6174G>A
  hgvsp: ENST00000367148.1:c.6174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6054G>A
  hgvsp: ENST00000346085.5:c.6054G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6015G>A
  hgvsp: ENST00000350026.5:c.6015G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4581G>A
  hgvsp: ENST00000414678.2:c.4581G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43804
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu2018Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-157528330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528330
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528330
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6175G>A
  hgvsp: ENSP00000356116.1:p.Val2059Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6001G>A
  hgvsp: ENSP00000275248.4:p.Val2001Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6016G>A
  hgvsp: ENSP00000055163.7:p.Val2006Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4582G>A
  hgvsp: ENSP00000412835.2:p.Val1528Ile
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6055G>A
  hgvsp: ENSP00000344546.4:p.Val2019Ile
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43802
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val2019Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-157528336-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528336
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528336
    reference: chr 6
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6181A>C
  hgvsp: ENST00000367148.1:c.6181A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6061A>C
  hgvsp: ENST00000346085.5:c.6061A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6007A>C
  hgvsp: ENST00000275248.4:c.6007A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6022A>C
  hgvsp: ENST00000350026.5:c.6022A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4588A>C
  hgvsp: ENST00000414678.2:c.4588A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43806
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg2021Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

6-157528337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528337
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528337
    reference: chr 6
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6062G>A
  hgvsp: ENSP00000344546.4:p.Arg2021Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6023G>A
  hgvsp: ENSP00000055163.7:p.Arg2008Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4589G>A
  hgvsp: ENSP00000412835.2:p.Arg1530Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6008G>A
  hgvsp: ENSP00000275248.4:p.Arg2003Lys
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6182G>A
  hgvsp: ENSP00000356116.1:p.Arg2061Lys
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg2021Lys
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: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

6-157528340-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528340
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528340
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6065A>G
  hgvsp: ENSP00000344546.4:p.Asp2022Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6185A>G
  hgvsp: ENSP00000356116.1:p.Asp2062Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6026A>G
  hgvsp: ENSP00000055163.7:p.Asp2009Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6011A>G
  hgvsp: ENSP00000275248.4:p.Asp2004Gly
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4592A>G
  hgvsp: ENSP00000412835.2:p.Asp1531Gly
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43811
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp2022Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

6-157528346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528346
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528346
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6071C>T
  hgvsp: ENSP00000344546.4:p.Thr2024Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6191C>T
  hgvsp: ENSP00000356116.1:p.Thr2064Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6017C>T
  hgvsp: ENSP00000275248.4:p.Thr2006Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4598C>T
  hgvsp: ENSP00000412835.2:p.Thr1533Met
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6032C>T
  hgvsp: ENSP00000055163.7:p.Thr2011Met
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9566
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43812
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr2024Met
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-157528347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528347
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528347
    reference: chr 6
allele count: 9
allele frequency: 7.412776331828814e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6018G>A
  hgvsp: ENST00000275248.4:c.6018G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6033G>A
  hgvsp: ENST00000350026.5:c.6033G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6192G>A
  hgvsp: ENST00000367148.1:c.6192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4599G>A
  hgvsp: ENST00000414678.2:c.4599G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6072G>A
  hgvsp: ENST00000346085.5:c.6072G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9567
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr2024Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD

6-157528348-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 157528348
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 157528348
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000412835
  ensembl transcript: ENST00000414678
  gene symbol: ARID1B
  hgvsc: ENST00000414678.2:c.4600T>C
  hgvsp: ENST00000414678.2:c.4600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000356116
  ensembl transcript: ENST00000367148
  gene symbol: ARID1B
  hgvsc: ENST00000367148.1:c.6193T>C
  hgvsp: ENST00000367148.1:c.6193T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000055163
  ensembl transcript: ENST00000350026
  gene symbol: ARID1B
  hgvsc: ENST00000350026.5:c.6034T>C
  hgvsp: ENST00000350026.5:c.6034T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000275248
  ensembl transcript: ENST00000275248
  gene symbol: ARID1B
  hgvsc: ENST00000275248.4:c.6019T>C
  hgvsp: ENST00000275248.4:c.6019T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049618
  ensembl protein: ENSP00000344546
  ensembl transcript: ENST00000346085
  gene symbol: ARID1B
  hgvsc: ENST00000346085.5:c.6073T>C
  hgvsp: ENST00000346085.5:c.6073T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18040
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43813
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu2025Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-32505316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505316
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505316
    reference: chr 8
allele count: 21
allele frequency: 1.749650069986003e-4
allele num: 120024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42115C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42115C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33234C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.80C>T
  hgvsp: ENSP00000433289.1:p.Pro27Leu
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42115C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30913C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22615
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15364
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro27Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

8-32505321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505321
    reference: chr 8
allele count: 5
allele frequency: 4.162088369460261e-5
allele num: 120132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.85C>T
  hgvsp: ENSP00000433289.1:p.Leu29Phe
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42120C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42120C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30918C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33239C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42120C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu29Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-32505323-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505323
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505323
    reference: chr 8
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33241T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.87T>C
  hgvsp: ENST00000520502.2:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42122T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30920T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42122T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42122T>C
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22637
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu29Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

8-32505334-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505334
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505334
    reference: chr 8
allele count: 3
allele frequency: 2.490784098834313e-5
allele num: 120444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42133C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42133C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.98C>G
  hgvsp: ENSP00000433289.1:p.Pro33Arg
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42133C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30931C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33252C>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro33Arg
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

8-32505335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505335
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505335
    reference: chr 8
allele count: 2
allele frequency: 1.659668398254029e-5
allele num: 120506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42134G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.99G>A
  hgvsp: ENST00000520502.2:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42134G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42134G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33253G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30932G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30932G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro33Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-32505337-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505337
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505337
    reference: chr 8
allele count: 541
allele frequency: 4.486573452090694e-3
allele num: 120582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42136C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.101C>A
  hgvsp: ENSP00000433289.1:p.Ala34Glu
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42136C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42136C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33255C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30934C>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15188
  bin: 2.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 4.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ala34Glu
num of homozygotes: 16
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

8-32505341-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505341
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505341
    reference: chr 8
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42140A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33259A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42140A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.105A>G
  hgvsp: ENST00000520502.2:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30938A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42140A>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-32505351-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505351
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505351
    reference: chr 8
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42150C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33269C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42150C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.115C>T
  hgvsp: ENSP00000433289.1:p.Pro39Ser
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42150C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30948C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30948C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22884
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro39Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-32505357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505357
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505357
    reference: chr 8
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.121C>T
  hgvsp: ENSP00000433289.1:p.Pro41Ser
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.1C>T
  hgvsp: ENSP00000433350.1:p.Pro1?
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42156C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33275C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42156C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30954C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42156C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1?
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

8-32505371-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505371
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505371
    reference: chr 8
allele count: 5
allele frequency: 4.129023733628421e-5
allele num: 121094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33289T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42170T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.135T>C
  hgvsp: ENST00000520502.2:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.15T>C
  hgvsp: ENST00000523041.1:c.15T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42170T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42170T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30968T>C
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23254
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp45Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-32505372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505372
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505372
    reference: chr 8
allele count: 635
allele frequency: 5.244639730417259e-3
allele num: 121076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42171G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.16G>A
  hgvsp: ENSP00000433350.1:p.Gly6Arg
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42171G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.136G>A
  hgvsp: ENSP00000433289.1:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30969G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42171G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33290G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 3.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 12435
  bin: 3.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
hgvs: p.Gly46Arg
num of homozygotes: 28
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

8-32505375-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505375
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505375
    reference: chr 8
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.19A>G
  hgvsp: ENSP00000433350.1:p.Arg7Gly
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42174A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.139A>G
  hgvsp: ENSP00000433289.1:p.Arg47Gly
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42174A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33293A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42174A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30972A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30972A>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg47Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/8-32505379-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505379
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505379
    reference: chr 8
allele count: 6
allele frequency: 4.952292911618079e-5
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.23C>A
  hgvsp: ENSP00000433350.1:p.Thr8Asn
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.143C>A
  hgvsp: ENSP00000433289.1:p.Thr48Asn
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42178C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33297C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42178C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30976C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42178C>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr48Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

8-32505382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505382
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505382
    reference: chr 8
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33300C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.146C>T
  hgvsp: ENSP00000433289.1:p.Pro49Leu
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.26C>T
  hgvsp: ENSP00000433350.1:p.Pro9Leu
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42181C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42181C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30979C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42181C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro49Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

8-32505386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505386
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505386
    reference: chr 8
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.30A>G
  hgvsp: ENST00000523041.1:c.30A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.150A>G
  hgvsp: ENST00000520502.2:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42185A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33304A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30983A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42185A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42185A>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly50Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

8-32505389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505389
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505389
    reference: chr 8
allele count: 32
allele frequency: 2.640307595834915e-4
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42188C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.33C>T
  hgvsp: ENST00000523041.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.153C>T
  hgvsp: ENST00000520502.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42188C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33307C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42188C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12619
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15530
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Leu51Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

8-32505390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505390
    reference: chr 8
allele count: 44
allele frequency: 3.629704179109402e-4
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42189G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.34G>A
  hgvsp: ENSP00000433350.1:p.Val12Met
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.154G>A
  hgvsp: ENSP00000433289.1:p.Val52Met
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42189G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33308G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42189G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30987G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12647
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Val52Met
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-32505390-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505390
    reference: chr 8
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433350
  ensembl transcript: ENST00000523041
  gene symbol: NRG1
  hgvsc: ENST00000523041.1:c.34G>C
  hgvsp: ENSP00000433350.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33308G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42189G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42189G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.154G>C
  hgvsp: ENSP00000433289.1:p.Val52Leu
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30987G>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42189G>C
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val52Leu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9448
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
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: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.75e-1

DP
type: SiteQuality
SIO_000300: 3.49166e6

MQ
type: SiteQuality
SIO_000300: 5.99e1

FS
type: SiteQuality
SIO_000300: 2.642e0

MQRankSum
type: SiteQuality
SIO_000300: -9.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.543e0

QD
type: SiteQuality
SIO_000300: 1.586e1

GenotypeQuality
all individuals: 1126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9443
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.123e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

DP
type: SiteQuality
SIO_000300: 3.491667e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e-1

QD
type: SiteQuality
SIO_000300: 1.428e1

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
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: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: -3.238e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 1.8377e1

DP
type: SiteQuality
SIO_000300: 3.491719e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e0

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

GenotypeQuality
all individuals: 43735
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9452
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
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: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: -3.238e0

QD
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 1.8377e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.491719e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

GenotypeQuality
all individuals: 1125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43737
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.692e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

DP
type: SiteQuality
SIO_000300: 3.491895e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

FS
type: SiteQuality
SIO_000300: 5.334e0

MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

GenotypeQuality
all individuals: 2008
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.167e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.492189e6

FS
type: SiteQuality
SIO_000300: 2.512e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.58e-1

GenotypeQuality
all individuals: 836
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 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: 10398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 3.49237e6

VQSLOD
type: SiteQuality
SIO_000300: -2.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: -9.01e-1

FS
type: SiteQuality
SIO_000300: 1.7071e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.228e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 816
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9374
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44045
bin: 9.75e1
variant carriers: 1208

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 16
allele frequency: 1.762114537444934e-2
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 65
allele frequency: 5.615065653075328e-3
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 1.538757453356415e-3
allele num: 10398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 78
allele frequency: 1.179316601149078e-2
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 204
allele frequency: 1.23546511627907e-2
allele num: 16512
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 842
allele frequency: 1.261839108020621e-2
allele num: 66728
num of homozygotes: 11

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

ReadPosRankSum
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SIO_000300: 6.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.765e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 5.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

DP
type: SiteQuality
SIO_000300: 3.593262e6

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

QD
type: SiteQuality
SIO_000300: 1.337e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.465e-1

DP
type: SiteQuality
SIO_000300: 3.507627e6

FS
type: SiteQuality
SIO_000300: 2.871e0

QD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1398e1

InbreedingCoeff
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: -3.8e-1

MQRankSum
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SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

QD
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SIO_000300: 1.353e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 2
allele frequency: 1.241773252204148e-4
allele num: 16106
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65310
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

FS
type: SiteQuality
SIO_000300: 6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.51e-1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.715298e6

QD
type: SiteQuality
SIO_000300: 1.547e1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.35e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.497e0

QD
type: SiteQuality
SIO_000300: 1.37e1

FS
type: SiteQuality
SIO_000300: 9.11e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

DP
type: SiteQuality
SIO_000300: 3.50786e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1106
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GenotypeQuality
all individuals: 1126
bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 3.78e0

FS
type: SiteQuality
SIO_000300: 4.4095e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.011e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.85e-1

DP
type: SiteQuality
SIO_000300: 3.507642e6

ClippingRankSum
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SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.129e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele count: 0
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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MQ
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele num: 8654
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.596798849024368e-4
allele num: 66726
num of homozygotes: 0

East Asian
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Latino
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Other
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South Asian
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allele num: 16512
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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FS
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MQRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele num: 8654
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66728
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10398
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European (Finnish)
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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ClippingRankSum
type: SiteQuality
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DP
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ReadPosRankSum
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FS
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8654
num of homozygotes: 0

European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66732
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South Asian
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Latino
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Other
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DP
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InbreedingCoeff
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QD
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -8.443e0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.938e1

VQSLOD
type: SiteQuality
SIO_000300: -4.914e0

DP
type: SiteQuality
SIO_000300: 3.507984e6

MQ
type: SiteQuality
SIO_000300: 5.277e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.216e1

DP
type: SiteQuality
SIO_000300: 3.508004e6

MQ
type: SiteQuality
SIO_000300: 5.241e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

FS
type: SiteQuality
SIO_000300: 4.7746e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.359999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.285e1

MQRankSum
type: SiteQuality
SIO_000300: -8.077e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 4.7443e1

DP
type: SiteQuality
SIO_000300: 3.508016e6

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.102e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 3.508093e6

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.31e1

FS
type: SiteQuality
SIO_000300: 1.428e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.299e1

QD
type: SiteQuality
SIO_000300: 2.206e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 4.4628e1

DP
type: SiteQuality
SIO_000300: 3.508112e6

MQRankSum
type: SiteQuality
SIO_000300: -7.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.801e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

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

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.508327e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 9.07e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e-1

QD
type: SiteQuality
SIO_000300: 4.97e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.545e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.029e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10404
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
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VQSLOD
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SIO_000300: 2.28e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66736
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Other
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African
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allele frequency: 1.922337562475971e-4
allele num: 10404
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South Asian
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Latino
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MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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European (Non-Finnish)
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allele num: 66736
num of homozygotes: 0

Latino
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Other
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African
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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African
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allele num: 10402
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European (Finnish)
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num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.946e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

MQRankSum
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
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SIO_000300: 2.0e-4

DP
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MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.702e1

MQ
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -8.997000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
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DP
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SIO_000300: 3.508593e6

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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DP
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MQ
type: SiteQuality
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FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 5.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.194e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.147e0

FS
type: SiteQuality
SIO_000300: 3.6469e1

DP
type: SiteQuality
SIO_000300: 3.508545e6

QD
type: SiteQuality
SIO_000300: 2.449e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

MQ
type: SiteQuality
SIO_000300: 5.527e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

Latino
type: Population
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

European (Finnish)
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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: 66732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.741e0

DP
type: SiteQuality
SIO_000300: 3.508797e6

QD
type: SiteQuality
SIO_000300: 1.455e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.735e0

QD
type: SiteQuality
SIO_000300: 9.23e0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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DP
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SIO_000300: 3.508681e6

MQRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 6
allele frequency: 6.933210076265311e-4
allele num: 8654
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10404
num of homozygotes: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

South Asian
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African
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allele num: 10404
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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ReadPosRankSum
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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SIO_000300: 6.76e-1

VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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num of homozygotes: 0

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

South Asian
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allele num: 16512
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African
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DP
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

East Asian
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African
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.508962e6

MQRankSum
type: SiteQuality
SIO_000300: -1.361e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

FS
type: SiteQuality
SIO_000300: 1.325e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.334e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 2018
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.271088513981974e-3
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 66738
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: 6.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 3.509204e6

FS
type: SiteQuality
SIO_000300: 5.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 43811
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1120
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.509157e6

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

QD
type: SiteQuality
SIO_000300: 1.321e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.509082e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.54e-1

FS
type: SiteQuality
SIO_000300: 5.491e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.6e1

FS
type: SiteQuality
SIO_000300: 6.791e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 3.509124e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9572
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.037e0

VQSLOD
type: SiteQuality
SIO_000300: -2.965e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.274e0

FS
type: SiteQuality
SIO_000300: 5.891e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: -1.068e0

QD
type: SiteQuality
SIO_000300: 1.504e1

DP
type: SiteQuality
SIO_000300: 3.509221e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Finnish)
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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: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.03e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.509098e6

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
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East Asian
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

African
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allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491759065028469e-5
allele num: 66740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
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SIO_000300: 1.3e0

ReadPosRankSum
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SIO_000300: 4.17e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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ClippingRankSum
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QD
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MQ
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SIO_000300: 5.956e1

DP
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VQSLOD
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SIO_000300: 2.09e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.764e0

DP
type: SiteQuality
SIO_000300: 3.509748e6

MQRankSum
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SIO_000300: 6.03e-1

VQSLOD
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SIO_000300: 9.21e-1

ReadPosRankSum
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SIO_000300: -3.84e-1

BaseQRankSum
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SIO_000300: 5.89e0

MQ
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SIO_000300: 5.975e1

QD
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SIO_000300: 1.36e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
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SIO_000300: 2.98e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 15
allele frequency: 9.1552734375e-4
allele num: 16384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.554840276934289e-5
allele num: 65864
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -2.181e0

MQRankSum
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SIO_000300: -1.6e-2

QD
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MQ
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FS
type: SiteQuality
SIO_000300: 2.422e0

InbreedingCoeff
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SIO_000300: -4.0e-4

ClippingRankSum
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.728383e6

ReadPosRankSum
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SIO_000300: 1.88e-1

VQSLOD
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SIO_000300: 2.6e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.044696139325295e-4
allele num: 16422
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.55e0

ReadPosRankSum
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SIO_000300: 6.900000000000001e-2

MQRankSum
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QD
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SIO_000300: 1.209e1

DP
type: SiteQuality
SIO_000300: 1.728383e6

FS
type: SiteQuality
SIO_000300: 1.546e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.798e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516162290011523e-5
allele num: 65956
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.154e1

FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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SIO_000300: 4.07e-1

MQ
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SIO_000300: 5.966e1

BaseQRankSum
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SIO_000300: 3.06e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.538440591812653e-5
allele num: 66102
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.512035805007863e-5
allele num: 66136
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Latino
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African
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South Asian
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Other
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European (Finnish)
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DP
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MQRankSum
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MQ
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FS
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1186
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variant carriers: 0

GenotypeQuality
all individuals: 8925
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 28
allele frequency: 2.422564457518602e-3
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 504
allele frequency: 4.917073170731708e-2
allele num: 10250
num of homozygotes: 16

Other
type: Population
allele count: 3
allele frequency: 3.31858407079646e-3
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.555837640160788e-5
allele num: 66174
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

DP
type: SiteQuality
SIO_000300: 1.738455e6

FS
type: SiteQuality
SIO_000300: 1.732e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.86e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.835e0

GenotypeDepth
all individuals: 15349
bin: 2.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9042
bin: 6.75e1
variant carriers: 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: 6598
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: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66266
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.723842862699339e-5
allele num: 10284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.033e0

FS
type: SiteQuality
SIO_000300: 8.747e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.509e0

MQRankSum
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SIO_000300: -1.017e0

VQSLOD
type: SiteQuality
SIO_000300: -1.449e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.927e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 1.11e1

DP
type: SiteQuality
SIO_000300: 1.73298e6

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1203
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.883e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

DP
type: SiteQuality
SIO_000300: 1.735615e6

QD
type: SiteQuality
SIO_000300: 1.923e1

GenotypeDepth
all individuals: 312
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
all individuals: 139
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variant carriers: 1

GenotypeDepth
all individuals: 4411
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GenotypeDepth
all individuals: 82
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 23
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GenotypeDepth
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GenotypeQuality
all individuals: 195
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GenotypeQuality
all individuals: 35856
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 9019
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GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 247
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GenotypeQuality
all individuals: 235
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GenotypeQuality
all individuals: 3442
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2291
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1203
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 2989
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66420
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: 6600
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.459e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 1.008e0

VQSLOD
type: SiteQuality
SIO_000300: 8.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.737894e6

QD
type: SiteQuality
SIO_000300: 1.613e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 294
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variant carriers: 0

GenotypeDepth
all individuals: 4419
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
all individuals: 2042
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variant carriers: 0

GenotypeDepth
all individuals: 83
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variant carriers: 1

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeDepth
all individuals: 24
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variant carriers: 1

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 257
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GenotypeQuality
all individuals: 84
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1023
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.513373805373565e-5
allele num: 66548
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: 6604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 1.299e1

DP
type: SiteQuality
SIO_000300: 1.743479e6

FS
type: SiteQuality
SIO_000300: 9.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

GenotypeDepth
all individuals: 55
bin: 9.75e1
variant carriers: 28

GenotypeDepth
all individuals: 15537
bin: 2.25e1
variant carriers: 8

GenotypeDepth
all individuals: 294
bin: 1.75e1
variant carriers: 7

GenotypeDepth
all individuals: 85
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variant carriers: 37

GenotypeDepth
all individuals: 142
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variant carriers: 2

GenotypeDepth
all individuals: 23133
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variant carriers: 18

GenotypeDepth
all individuals: 2068
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variant carriers: 67

GenotypeDepth
all individuals: 126
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variant carriers: 48

GenotypeDepth
all individuals: 37
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variant carriers: 17

GenotypeDepth
all individuals: 13
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variant carriers: 6

GenotypeQuality
all individuals: 9025
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GenotypeQuality
all individuals: 2234
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 603

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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variant carriers: 1

South Asian
type: Population
allele count: 14
allele frequency: 8.48073661255149e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00543984612148e-5
allele num: 66546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.897990726429675e-4
allele num: 10352
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 609
allele frequency: 7.074814126394052e-2
allele num: 8608
num of homozygotes: 28

Other
type: Population
allele count: 6
allele frequency: 6.622516556291391e-3
allele num: 906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.44e-2

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

DP
type: SiteQuality
SIO_000300: 1.759126e6

GenotypeDepth
all individuals: 198
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 2.868e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.94e-1

ReadPosRankSum
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SIO_000300: -1.071e0

QD
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SIO_000300: 7.81e0

MQRankSum
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SIO_000300: -1.601e0

DP
type: SiteQuality
SIO_000300: 1.744857e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.011173855580921e-5
allele num: 66584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQRankSum
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SIO_000300: -4.35e-1

BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 1.179e0

ClippingRankSum
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SIO_000300: -3.82e-1

DP
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SIO_000300: 1.746061e6

VQSLOD
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SIO_000300: 1.95e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

FS
type: SiteQuality
SIO_000300: 7.565e0

InbreedingCoeff
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SIO_000300: 5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

BaseQRankSum
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SIO_000300: -2.576e0

DP
type: SiteQuality
SIO_000300: 1.746739e6

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 5.7e-3

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

VQSLOD
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FS
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SIO_000300: 6.411e0

QD
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

DP
type: SiteQuality
SIO_000300: 1.747825e6

GenotypeDepth
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variant carriers: 6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 30
allele frequency: 2.892402622445044e-3
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

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

South Asian
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allele count: 0
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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Latino
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allele num: 11554
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African
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allele count: 42
allele frequency: 4.048582995951417e-3
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.500870504892838e-5
allele num: 66628
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South Asian
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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