7-150749346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749346
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749346
    reference: chr 7
allele count: 2
allele frequency: 1.654971534489607e-5
allele num: 120848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*86+22C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1458+22C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.352C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.335+22C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1458+22C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*108C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+22C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3419
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8217
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-150749348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749348
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749348
    reference: chr 7
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.351+24C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.354C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1458+24C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.335+24C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*110C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*86+24C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1458+24C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+24C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4237
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

7-150749351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749351
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749351
    reference: chr 7
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*113G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.351+27G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*86+27G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+27G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1458+27G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.357G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1458+27G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.335+27G>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

7-150749351-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749351
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749351
    reference: chr 7
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.335+27G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1458+27G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.351+27G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*86+27G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.357G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*113G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1458+27G>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+27G>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8084
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-150749373-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749373
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749373
    reference: chr 7
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*86+49C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.351+49C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*135C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1458+49C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.335+49C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+49C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.379C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1458+49C>G
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8217
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

7-150749374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749374
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749374
    reference: chr 7
allele count: 1
allele frequency: 8.287063893262618e-6
allele num: 120670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1458+50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1458+50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*136C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.351+50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.380C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.335+50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*86+50C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6787
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-150749453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749453
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749453
    reference: chr 7
allele count: 1
allele frequency: 8.265692417053776e-6
allele num: 120982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.459C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+129C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-50C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*215C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-50C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41126
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum

7-150749459-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749459
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749459
    reference: chr 7
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-44G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*221G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.465G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-44G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-44G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-44G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-44G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+135G>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5850
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

7-150749464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749464
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749464
    reference: chr 7
allele count: 1
allele frequency: 8.264462809917356e-6
allele num: 121000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.470G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*226G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-39G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-39G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-39G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+140G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-39G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-39G>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

7-150749469-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749469
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749469
    reference: chr 7
allele count: 349
allele frequency: 2.883534932910305e-3
allele num: 121032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-34A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-34A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+145A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-34A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.475A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-34A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-34A>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*231A>G
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 9.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6345
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 9.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 6.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 5
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

7-150749471-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749471
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749471
    reference: chr 7
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.477T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-32T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-32T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-32T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-32T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*233T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+147T>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-32T>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2669
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-150749472-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749472
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749472
    reference: chr 7
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*234C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-31C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.478C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+148C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-31C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-31C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-31C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-31C>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-150749475-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749475
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749475
    reference: chr 7
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-28C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-28C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-28C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-28C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+151C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-28C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*237C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.481C>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1919
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

7-150749479-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749479
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749479
    reference: chr 7
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*241T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-24T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.485T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+155T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-24T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-24T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-24T>C
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-24T>C
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/7-150749484-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749484
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749484
    reference: chr 7
allele count: 2
allele frequency: 1.651364026686043e-5
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-19C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-19C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.490C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-19C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*246C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+160C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-19C>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-19C>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6882
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41046
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum

7-150749485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749485
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749485
    reference: chr 7
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-18C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+161C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*247C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-18C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-18C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.491C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-18C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-18C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41047
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6886
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

7-150749485-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749485
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749483
    reference: chr 7
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-14_*87-13delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-14_336-13delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*251_*252delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-14_1459-13delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.495_496delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-14_352-13delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+165_1458+166delTC
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-14_1459-13delTC
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1540
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: CCT
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

7-150749490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749490
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749490
    reference: chr 7
allele count: 74
allele frequency: 6.109138941632956e-4
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.496C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-13C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-13C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-13C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-13C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*252C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-13C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1458+166C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

7-150749494-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749494
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749494
    reference: chr 7
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459-9C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-167C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.500C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459-9C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87-9C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352-9C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*256C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336-9C>G
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-150749503-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749503
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749503
    reference: chr 7
allele count: 26
allele frequency: 2.145816483171847e-4
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-158C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*265C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.352C>T
  hgvsp: ENSP00000418361.1:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1459C>T
  hgvsp: ENSP00000297512.8:p.Leu487Phe
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.336C>T
  hgvsp: ENSP00000420371.1:p.Leu113Phe
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1459C>T
  hgvsp: ENSP00000344838.5:p.Leu487Phe
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*87C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.509C>T
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu487Phe
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

7-150749513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749513
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749513
    reference: chr 7
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1469G>A
  hgvsp: ENSP00000344838.5:p.Gly490Glu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1469G>A
  hgvsp: ENSP00000297512.8:p.Gly490Glu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*275G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-148G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.346G>A
  hgvsp: ENSP00000420371.1:p.Gly116Glu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.519G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.362G>A
  hgvsp: ENSP00000418361.1:p.Gly121Glu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly490Glu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

7-150749522-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749522
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749522
    reference: chr 7
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*106G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-139G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.528G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1478G>A
  hgvsp: ENSP00000344838.5:p.Ser493Asn
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.371G>A
  hgvsp: ENSP00000418361.1:p.Ser124Asn
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.355G>A
  hgvsp: ENSP00000420371.1:p.Ser119Asn
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*284G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1478G>A
  hgvsp: ENSP00000297512.8:p.Ser493Asn
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser493Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-150749527-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749527
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749527
    reference: chr 7
allele count: 4
allele frequency: 3.30016665841625e-5
allele num: 121206
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1483C>G
  hgvsp: ENSP00000297512.8:p.Arg495Gly
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.533C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-134C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*289C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*111C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.360C>G
  hgvsp: ENSP00000420371.1:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.376C>G
  hgvsp: ENSP00000418361.1:p.Arg126Gly
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1483C>G
  hgvsp: ENSP00000344838.5:p.Arg495Gly
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg495Gly
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-150749527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749527
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749527
    reference: chr 7
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1483C>T
  hgvsp: ENSP00000344838.5:p.Arg495Ter
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.360C>T
  hgvsp: ENSP00000420371.1:p.Arg121Ter
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.376C>T
  hgvsp: ENSP00000418361.1:p.Arg126Ter
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*289C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-134C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*111C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1483C>T
  hgvsp: ENSP00000297512.8:p.Arg495Ter
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.533C>T
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41028
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg495Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

7-150749528-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749528
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749528
    reference: chr 7
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1484G>A
  hgvsp: ENSP00000297512.8:p.Arg495Gln
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.377G>A
  hgvsp: ENSP00000418361.1:p.Arg126Gln
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*290G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.361G>A
  hgvsp: ENSP00000420371.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.534G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1484G>A
  hgvsp: ENSP00000344838.5:p.Arg495Gln
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-133G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*112G>A
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg495Gln
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

7-150749532-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749532
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749532
    reference: chr 7
allele count: 3
allele frequency: 2.475002475002475e-5
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1488C>G
  hgvsp: ENST00000349064.5:c.1488C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.381C>G
  hgvsp: ENST00000490540.1:c.381C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1488C>G
  hgvsp: ENST00000297512.8:c.1488C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*294C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.365C>G
  hgvsp: ENST00000485929.1:c.365C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-129C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*116C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.538C>G
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41028
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr496Thr
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

7-150749532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749532
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749532
    reference: chr 7
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.381C>T
  hgvsp: ENST00000490540.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-129C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1488C>T
  hgvsp: ENST00000297512.8:c.1488C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*116C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.538C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1488C>T
  hgvsp: ENST00000349064.5:c.1488C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.365C>T
  hgvsp: ENST00000485929.1:c.365C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*294C>T
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr496Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/7-150749533-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749533
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749534
    reference: chr 7
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1491dupA
  hgvsp: ENSP00000344838.5:p.Val498SerfsTer67
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*119dupA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*297dupA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-126dupA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1491dupA
  hgvsp: ENSP00000297512.8:p.Val498SerfsTer42
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.384dupA
  hgvsp: ENSP00000418361.1:p.Val129SerfsTer11
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.368dupA
  hgvsp: ENSP00000420371.1:p.Val124SerfsTer11
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.541dupA
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7197
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val498SerfsTer42
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-150749540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749540
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749540
    reference: chr 7
allele count: 5
allele frequency: 4.125684863687372e-5
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.373C>T
  hgvsp: ENSP00000420371.1:p.Pro125Leu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1496C>T
  hgvsp: ENSP00000344838.5:p.Pro499Leu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*302C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.389C>T
  hgvsp: ENSP00000418361.1:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-121C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1496C>T
  hgvsp: ENSP00000297512.8:p.Pro499Leu
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*124C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.546C>T
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro499Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

7-150749555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749555
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749555
    reference: chr 7
allele count: 2
allele frequency: 1.650546330835507e-5
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1511G>A
  hgvsp: ENSP00000297512.8:p.Gly504Asp
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.404G>A
  hgvsp: ENSP00000418361.1:p.Gly135Asp
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1511G>A
  hgvsp: ENSP00000344838.5:p.Gly504Asp
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*139G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*317G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.388G>A
  hgvsp: ENSP00000420371.1:p.Gly130Asp
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.561G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-106G>A
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2749
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41020
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly504Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

7-150749559-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749559
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749559
    reference: chr 7
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.408C>T
  hgvsp: ENST00000490540.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.392C>T
  hgvsp: ENST00000485929.1:c.392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*321C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1515C>T
  hgvsp: ENST00000349064.5:c.1515C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1515C>T
  hgvsp: ENST00000297512.8:c.1515C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-102C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.565C>T
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41017
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1515C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

7-108137020-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137020
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137020
    reference: chr 7
allele count: 8
allele frequency: 6.803068183750872e-5
allele num: 117594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1625+8A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1325+8A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1625+8A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1325+8A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1625+8A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1625+8A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.562A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1625+8A>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1625+8A>G
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

7-150749561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749561
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749561
    reference: chr 7
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517G>A
  hgvsp: ENSP00000297512.8:p.Ser506Asn
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517G>A
  hgvsp: ENSP00000344838.5:p.Arg506Lys
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-100G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410G>A
  hgvsp: ENSP00000418361.1:p.Ser137Asn
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.567G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394G>A
  hgvsp: ENSP00000420371.1:p.Ser132Asn
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145G>A
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser506Asn
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

7-150749566-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749566
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749566
    reference: chr 7
allele count: 77
allele frequency: 6.355967180096743e-4
allele num: 121146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+5C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+5C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+5C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-95C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+5C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+5C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.572C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+5C>T
  variant of: http://identifiers.org/hgnc/101
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 8.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1517+5C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

7-150749574-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749574
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749574
    reference: chr 7
allele count: 7
allele frequency: 5.780346820809248e-5
allele num: 121100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+13G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+13G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.580G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+13G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-87G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+13G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+13G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+13G>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

7-150749575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749575
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749575
    reference: chr 7
allele count: 5
allele frequency: 4.129023733628421e-5
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+14G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.581G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+14G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+14G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+14G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+14G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+14G>A
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-86G>A
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6555
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum

7-150749577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749577
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749577
    reference: chr 7
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.583C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+16C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+16C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+16C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+16C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-84C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+16C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+16C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

7-150749578-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749578
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749578
    reference: chr 7
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+17C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+17C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+17C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+17C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+17C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.584C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+17C>G
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-83C>G
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6500
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

7-150749580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749580
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749580
    reference: chr 7
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+19C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-81C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+19C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+19C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+19C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.586C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+19C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+19C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2633
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40983
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

7-150749592-GAGGGCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749592
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749586
    reference: chr 7
allele count: 3
allele frequency: 2.4786833234186e-5
allele num: 121032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-68_1459-63delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+32_410+37delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+32_1517+37delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.599_604delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+32_394+37delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+32_*323+37delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+32_*145+37delAGGGCA
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+32_1517+37delAGGGCA
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: GAGGGCA
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD

7-150749597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150749597
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 150749597
    reference: chr 7
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000420371
  ensembl transcript: ENST00000485929
  gene symbol: ASIC3
  hgvsc: ENST00000485929.1:c.394+36C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000297512
  ensembl transcript: ENST00000297512
  gene symbol: ASIC3
  hgvsc: ENST00000297512.8:c.1517+36C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418361
  ensembl transcript: ENST00000490540
  gene symbol: ASIC3
  hgvsc: ENST00000490540.1:c.410+36C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000344838
  ensembl transcript: ENST00000349064
  gene symbol: ASIC3
  hgvsc: ENST00000349064.5:c.1517+36C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000367136
  ensembl transcript: ENST00000377904
  gene symbol: ASIC3
  hgvsc: ENST00000377904.4:c.*323+36C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213199
  ensembl transcript: ENST00000498105
  gene symbol: ASIC3
  hgvsc: ENST00000498105.1:n.603C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000418605
  ensembl transcript: ENST00000468325
  gene symbol: ASIC3
  hgvsc: ENST00000468325.1:c.*145+36C>T
  variant of: http://identifiers.org/hgnc/101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213199
  ensembl protein: ENSP00000350600
  ensembl transcript: ENST00000357922
  gene symbol: ASIC3
  hgvsc: ENST00000357922.4:c.1459-64C>T
  variant of: http://identifiers.org/hgnc/101
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40975
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

7-108137021-AACTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137021
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137017
    reference: chr 7
allele count: 1
allele frequency: 8.482915408367548e-6
allele num: 117884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1325+3_1325+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1625+3_1625+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1325+3_1325+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1625+3_1625+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1625+3_1625+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1625+3_1625+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.557_560delAAGT
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1625+3_1625+6delAAGT
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1625+3_1625+6delAAGT
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: AACTT
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

7-108137038-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137038
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137038
    reference: chr 7
allele count: 53
allele frequency: 4.404846993899702e-4
allele num: 120322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1615A>G
  hgvsp: ENSP00000257694.8:p.Asn539Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1615A>G
  hgvsp: ENSP00000406779.1:p.Asn539Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1315A>G
  hgvsp: ENSP00000387789.1:p.Asn439Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1615A>G
  hgvsp: ENSP00000394988.2:p.Asn539Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.555A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1615A>G
  hgvsp: ENSP00000410804.1:p.Asn539Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1315A>G
  hgvsp: ENSP00000402274.1:p.Asn439Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.651A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1615A>G
  hgvsp: ENSP00000373380.5:p.Asn539Asp
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.544A>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39420
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11066
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn539Asp
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

7-108137043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137043
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137043
    reference: chr 7
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1610G>A
  hgvsp: ENSP00000257694.8:p.Trp537Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1610G>A
  hgvsp: ENSP00000406779.1:p.Trp537Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1610G>A
  hgvsp: ENSP00000394988.2:p.Trp537Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.646G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1310G>A
  hgvsp: ENSP00000387789.1:p.Trp437Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1610G>A
  hgvsp: ENSP00000410804.1:p.Trp537Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.539G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.550G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1610G>A
  hgvsp: ENSP00000373380.5:p.Trp537Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1310G>A
  hgvsp: ENSP00000402274.1:p.Trp437Ter
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Trp537Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ

7-108137072-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137072
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137072
    reference: chr 7
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1581G>A
  hgvsp: ENSP00000257694.8:p.Trp527Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1281G>A
  hgvsp: ENSP00000387789.1:p.Trp427Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.521G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1281G>A
  hgvsp: ENSP00000402274.1:p.Trp427Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.510G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.617G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1581G>A
  hgvsp: ENSP00000394988.2:p.Trp527Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1581G>A
  hgvsp: ENSP00000410804.1:p.Trp527Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1581G>A
  hgvsp: ENSP00000406779.1:p.Trp527Ter
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1581G>A
  hgvsp: ENSP00000373380.5:p.Trp527Ter
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Trp527Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

7-108137097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137097
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137097
    reference: chr 7
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1556T>C
  hgvsp: ENSP00000410804.1:p.Ile519Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1556T>C
  hgvsp: ENSP00000257694.8:p.Ile519Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1256T>C
  hgvsp: ENSP00000402274.1:p.Ile419Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.592T>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.496T>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1556T>C
  hgvsp: ENSP00000406779.1:p.Ile519Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1256T>C
  hgvsp: ENSP00000387789.1:p.Ile419Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1556T>C
  hgvsp: ENSP00000394988.2:p.Ile519Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1556T>C
  hgvsp: ENSP00000373380.5:p.Ile519Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.485T>C
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile519Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

7-108137098-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137098
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137098
    reference: chr 7
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1555A>G
  hgvsp: ENSP00000373380.5:p.Ile519Val
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1555A>G
  hgvsp: ENSP00000257694.8:p.Ile519Val
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1255A>G
  hgvsp: ENSP00000387789.1:p.Ile419Val
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.495A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1555A>G
  hgvsp: ENSP00000394988.2:p.Ile519Val
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1255A>G
  hgvsp: ENSP00000402274.1:p.Ile419Val
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1555A>G
  hgvsp: ENSP00000406779.1:p.Ile519Val
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.484A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.591A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1555A>G
  hgvsp: ENSP00000410804.1:p.Ile519Val
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile519Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

7-108137099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137099
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137099
    reference: chr 7
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1554C>T
  hgvsp: ENST00000257694.8:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1554C>T
  hgvsp: ENST00000426128.2:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.483C>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1254C>T
  hgvsp: ENST00000453144.1:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1554C>T
  hgvsp: ENST00000388728.5:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1254C>T
  hgvsp: ENST00000453085.1:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.494C>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1554C>T
  hgvsp: ENST00000422087.1:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.590C>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1554C>T
  hgvsp: ENST00000436062.1:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val518Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

7-108137103-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137103
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137103
    reference: chr 7
allele count: 12
allele frequency: 9.904585823236159e-5
allele num: 121156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1550A>G
  hgvsp: ENSP00000257694.8:p.Asn517Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.586A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1250A>G
  hgvsp: ENSP00000387789.1:p.Asn417Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1550A>G
  hgvsp: ENSP00000406779.1:p.Asn517Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1550A>G
  hgvsp: ENSP00000373380.5:p.Asn517Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1550A>G
  hgvsp: ENSP00000410804.1:p.Asn517Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.479A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1250A>G
  hgvsp: ENSP00000402274.1:p.Asn417Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.490A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1550A>G
  hgvsp: ENSP00000394988.2:p.Asn517Ser
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn517Ser
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

7-108137106-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137106
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137106
    reference: chr 7
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1547A>G
  hgvsp: ENSP00000410804.1:p.Gln516Arg
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1547A>G
  hgvsp: ENSP00000373380.5:p.Gln516Arg
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1247A>G
  hgvsp: ENSP00000402274.1:p.Gln416Arg
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.476A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1547A>G
  hgvsp: ENSP00000394988.2:p.Gln516Arg
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.487A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1547A>G
  hgvsp: ENSP00000406779.1:p.Gln516Arg
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.583A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1247A>G
  hgvsp: ENSP00000387789.1:p.Gln416Arg
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1547A>G
  hgvsp: ENSP00000257694.8:p.Gln516Arg
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln516Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

7-108137133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137133
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137133
    reference: chr 7
allele count: 3
allele frequency: 2.47618733182561e-5
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1520G>A
  hgvsp: ENSP00000406779.1:p.Arg507Gln
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1520G>A
  hgvsp: ENSP00000373380.5:p.Arg507Gln
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.449G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1520G>A
  hgvsp: ENSP00000257694.8:p.Arg507Gln
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.460G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1520G>A
  hgvsp: ENSP00000410804.1:p.Arg507Gln
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.556G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1520G>A
  hgvsp: ENSP00000394988.2:p.Arg507Gln
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1220G>A
  hgvsp: ENSP00000387789.1:p.Arg407Gln
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1220G>A
  hgvsp: ENSP00000402274.1:p.Arg407Gln
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg507Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

7-108137149-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137149
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137149
    reference: chr 7
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1504T>A
  hgvsp: ENSP00000373380.5:p.Cys502Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1504T>A
  hgvsp: ENSP00000394988.2:p.Cys502Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1204T>A
  hgvsp: ENSP00000402274.1:p.Cys402Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.433T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1504T>A
  hgvsp: ENSP00000410804.1:p.Cys502Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.540T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1204T>A
  hgvsp: ENSP00000387789.1:p.Cys402Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1504T>A
  hgvsp: ENSP00000406779.1:p.Cys502Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1504T>A
  hgvsp: ENSP00000257694.8:p.Cys502Ser
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.444T>A
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys502Ser
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: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

7-108137154-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137154
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137154
    reference: chr 7
allele count: 1
allele frequency: 8.256411103221652e-6
allele num: 121118
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1499A>G
  hgvsp: ENSP00000410804.1:p.Asp500Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.439A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.535A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.428A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1199A>G
  hgvsp: ENSP00000387789.1:p.Asp400Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1499A>G
  hgvsp: ENSP00000406779.1:p.Asp500Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1499A>G
  hgvsp: ENSP00000257694.8:p.Asp500Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1499A>G
  hgvsp: ENSP00000394988.2:p.Asp500Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1199A>G
  hgvsp: ENSP00000402274.1:p.Asp400Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1499A>G
  hgvsp: ENSP00000373380.5:p.Asp500Gly
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp500Gly
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

7-108137155-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137155
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137155
    reference: chr 7
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.534G>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1498G>C
  hgvsp: ENSP00000394988.2:p.Asp500His
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1498G>C
  hgvsp: ENSP00000410804.1:p.Asp500His
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1198G>C
  hgvsp: ENSP00000387789.1:p.Asp400His
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.427G>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1498G>C
  hgvsp: ENSP00000406779.1:p.Asp500His
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1198G>C
  hgvsp: ENSP00000402274.1:p.Asp400His
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1498G>C
  hgvsp: ENSP00000257694.8:p.Asp500His
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.438G>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1498G>C
  hgvsp: ENSP00000373380.5:p.Asp500His
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp500His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-108137163-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137163
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137163
    reference: chr 7
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1490T>C
  hgvsp: ENSP00000257694.8:p.Met497Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.430T>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1190T>C
  hgvsp: ENSP00000402274.1:p.Met397Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1490T>C
  hgvsp: ENSP00000394988.2:p.Met497Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1490T>C
  hgvsp: ENSP00000410804.1:p.Met497Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.526T>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1490T>C
  hgvsp: ENSP00000373380.5:p.Met497Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1190T>C
  hgvsp: ENSP00000387789.1:p.Met397Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1490T>C
  hgvsp: ENSP00000406779.1:p.Met497Thr
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.419T>C
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met497Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

7-108137174-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137174
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137174
    reference: chr 7
allele count: 6
allele frequency: 4.958349861166204e-5
allele num: 121008
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1479G>C
  hgvsp: ENST00000257694.8:c.1479G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.419G>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.408G>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1479G>C
  hgvsp: ENST00000426128.2:c.1479G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1179G>C
  hgvsp: ENST00000453144.1:c.1179G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1479G>C
  hgvsp: ENST00000422087.1:c.1479G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1179G>C
  hgvsp: ENST00000453085.1:c.1179G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1479G>C
  hgvsp: ENST00000388728.5:c.1479G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.515G>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1479G>C
  hgvsp: ENST00000436062.1:c.1479G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly493Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-108137180-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137180
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137180
    reference: chr 7
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.402G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1473G>T
  hgvsp: ENSP00000257694.8:p.Met491Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1173G>T
  hgvsp: ENSP00000402274.1:p.Met391Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1173G>T
  hgvsp: ENSP00000387789.1:p.Met391Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1473G>T
  hgvsp: ENSP00000410804.1:p.Met491Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1473G>T
  hgvsp: ENSP00000373380.5:p.Met491Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1473G>T
  hgvsp: ENSP00000394988.2:p.Met491Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1473G>T
  hgvsp: ENSP00000406779.1:p.Met491Ile
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.509G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.413G>T
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met491Ile
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

7-108137182-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137182
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137182
    reference: chr 7
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1471A>T
  hgvsp: ENSP00000394988.2:p.Met491Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.400A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.411A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1471A>T
  hgvsp: ENSP00000406779.1:p.Met491Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1471A>T
  hgvsp: ENSP00000373380.5:p.Met491Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1171A>T
  hgvsp: ENSP00000387789.1:p.Met391Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1471A>T
  hgvsp: ENSP00000257694.8:p.Met491Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1471A>T
  hgvsp: ENSP00000410804.1:p.Met491Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1171A>T
  hgvsp: ENSP00000402274.1:p.Met391Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.507A>T
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met491Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

7-108137187-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137187
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137187
    reference: chr 7
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1466C>G
  hgvsp: ENSP00000373380.5:p.Ala489Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1466C>G
  hgvsp: ENSP00000257694.8:p.Ala489Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1466C>G
  hgvsp: ENSP00000394988.2:p.Ala489Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1166C>G
  hgvsp: ENSP00000402274.1:p.Ala389Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1466C>G
  hgvsp: ENSP00000410804.1:p.Ala489Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1466C>G
  hgvsp: ENSP00000406779.1:p.Ala489Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1166C>G
  hgvsp: ENSP00000387789.1:p.Ala389Gly
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.502C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.395C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.406C>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala489Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

7-108137194-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137194
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137194
    reference: chr 7
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1159A>T
  hgvsp: ENSP00000402274.1:p.Ile387Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1459A>T
  hgvsp: ENSP00000257694.8:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1159A>T
  hgvsp: ENSP00000387789.1:p.Ile387Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1459A>T
  hgvsp: ENSP00000394988.2:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1459A>T
  hgvsp: ENSP00000410804.1:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1459A>T
  hgvsp: ENSP00000373380.5:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1459A>T
  hgvsp: ENSP00000406779.1:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.388A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.399A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.495A>T
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile487Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-108137194-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137194
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137194
    reference: chr 7
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.399A>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1459A>C
  hgvsp: ENSP00000410804.1:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.495A>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.388A>C
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1159A>C
  hgvsp: ENSP00000387789.1:p.Ile387Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1459A>C
  hgvsp: ENSP00000406779.1:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1159A>C
  hgvsp: ENSP00000402274.1:p.Ile387Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1459A>C
  hgvsp: ENSP00000257694.8:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1459A>C
  hgvsp: ENSP00000373380.5:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1459A>C
  hgvsp: ENSP00000394988.2:p.Ile487Leu
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile487Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-108137209-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137209
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137209
    reference: chr 7
allele count: 7
allele frequency: 5.829349944204793e-5
allele num: 120082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-10T>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-10T>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11790
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44641
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5349
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

7-108137210-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137210
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137210
    reference: chr 7
allele count: 1
allele frequency: 8.3301401129567e-6
allele num: 120046
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-11C>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-11C>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4493
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

7-108137212-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137212
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137212
    reference: chr 7
allele count: 2
allele frequency: 1.666638889351844e-5
allele num: 120002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-13T>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-13T>A
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31850
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43851
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-108137233-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137233
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137233
    reference: chr 7
allele count: 1
allele frequency: 8.658008658008657e-6
allele num: 115500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-34A>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-34A>T
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
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: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum

7-108137240-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137240
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137240
    reference: chr 7
allele count: 2
allele frequency: 2.003245257316853e-5
allele num: 99838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-41A>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17692
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-108137243-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137243
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137243
    reference: chr 7
allele count: 2
allele frequency: 2.399002015161693e-5
allele num: 83368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-44G>T
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-44G>T
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8421
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15988
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

7-108137245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137245
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137245
    reference: chr 7
allele count: 1
allele frequency: 1.665278934221482e-5
allele num: 60050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.394-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1454-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1154-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.490-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1154-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1454-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1454-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.383-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1454-46G>A
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1454-46G>A
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8907
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

7-108137883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137883
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137883
    reference: chr 7
allele count: 1
allele frequency: 8.550955141689327e-6
allele num: 116946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1153+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.489+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1453+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.393+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1153+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.382+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1453+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1453+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1453+44A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1453+44A>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

7-108137886-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108137886
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 108137886
    reference: chr 7
allele count: 4
allele frequency: 3.41646737273659e-5
allele num: 117080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000483879
  gene symbol: PNPLA8
  hgvsc: ENST00000483879.1:n.382+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000373380
  ensembl transcript: ENST00000388728
  gene symbol: PNPLA8
  hgvsc: ENST00000388728.5:c.1453+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000257694
  ensembl transcript: ENST00000257694
  gene symbol: PNPLA8
  hgvsc: ENST00000257694.8:c.1453+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000462466
  gene symbol: PNPLA8
  hgvsc: ENST00000462466.1:n.393+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000402274
  ensembl transcript: ENST00000453085
  gene symbol: PNPLA8
  hgvsc: ENST00000453085.1:c.1153+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000410804
  ensembl transcript: ENST00000422087
  gene symbol: PNPLA8
  hgvsc: ENST00000422087.1:c.1453+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000387789
  ensembl transcript: ENST00000453144
  gene symbol: PNPLA8
  hgvsc: ENST00000453144.1:c.1153+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000406779
  ensembl transcript: ENST00000436062
  gene symbol: PNPLA8
  hgvsc: ENST00000436062.1:c.1453+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl protein: ENSP00000394988
  ensembl transcript: ENST00000426128
  gene symbol: PNPLA8
  hgvsc: ENST00000426128.2:c.1453+41A>G
  variant of: http://identifiers.org/hgnc/28900
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135241
  ensembl transcript: ENST00000476592
  gene symbol: PNPLA8
  hgvsc: ENST00000476592.1:n.489+41A>G
  variant of: http://identifiers.org/hgnc/28900
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21887
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32156
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.01559060341968e-5
allele num: 66322
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: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.55e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

DP
type: SiteQuality
SIO_000300: 2.622676e6

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32156
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8156
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
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: 10302
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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: 1.507749834147518e-5
allele num: 66324
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-2

FS
type: SiteQuality
SIO_000300: 1.007e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.025e0

DP
type: SiteQuality
SIO_000300: 2.621697e6

GenotypeQuality
all individuals: 4226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8084
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32154
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
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: 0
allele frequency: 0.0e0
allele num: 16494
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: 1.508341126429153e-5
allele num: 66298
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.686e0

FS
type: SiteQuality
SIO_000300: 3.379e0

VQSLOD
type: SiteQuality
SIO_000300: 6.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.338e1

DP
type: SiteQuality
SIO_000300: 2.620476e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

GenotypeQuality
all individuals: 233
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32154
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
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: 10300
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 3.379e0

QD
type: SiteQuality
SIO_000300: 1.338e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.686e0

DP
type: SiteQuality
SIO_000300: 2.620476e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32156
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

East Asian
type: Population
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: 10262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66200
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: 11570
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.793e0

QD
type: SiteQuality
SIO_000300: 1.628e1

VQSLOD
type: SiteQuality
SIO_000300: -9.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.610513e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4095
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
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: 66198
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.852e0

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.443e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 1.062e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e0

DP
type: SiteQuality
SIO_000300: 2.610408e6

GenotypeQuality
all individuals: 348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2641
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 3.16518e6

MQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.446e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

QD
type: SiteQuality
SIO_000300: 1.352e1

FS
type: SiteQuality
SIO_000300: 2.548e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.255e0

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41116
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505298651252408e-5
allele num: 66432
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.961e0

DP
type: SiteQuality
SIO_000300: 3.165605e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.235e0

VQSLOD
type: SiteQuality
SIO_000300: -2.412e0

FS
type: SiteQuality
SIO_000300: 7.718e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.56e0

GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41113
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1930
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2088
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6135
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.672e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

DP
type: SiteQuality
SIO_000300: 3.166601e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

FS
type: SiteQuality
SIO_000300: 6.26e0

QD
type: SiteQuality
SIO_000300: 1.418e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41160
bin: 9.75e1
variant carriers: 342

GenotypeQuality
all individuals: 1527
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6371
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 9
allele frequency: 7.777393708952644e-4
allele num: 11572
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: 332
allele frequency: 3.195380173243503e-2
allele num: 10390
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.019925954910755e-5
allele num: 66446
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.325942350332594e-3
allele num: 902
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.65e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.269e0

DP
type: SiteQuality
SIO_000300: 3.171013e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.241e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

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

GenotypeQuality
all individuals: 2121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41050
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6455
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variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
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: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504890895410083e-5
allele num: 66450
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.01e1

FS
type: SiteQuality
SIO_000300: 8.8e-1

DP
type: SiteQuality
SIO_000300: 3.163741e6

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.396e0

GenotypeQuality
all individuals: 2119
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2095
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41050
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6531
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.754e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 9.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 3.164381e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.59e-1

GenotypeQuality
all individuals: 1625
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41048
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6641
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

DP
type: SiteQuality
SIO_000300: 3.165382e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 9.01e0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

GenotypeQuality
all individuals: 240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 2122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41046
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
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variant carriers: 0

GenotypeQuality
all individuals: 1920
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 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: 8646
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: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.452e1

VQSLOD
type: SiteQuality
SIO_000300: -1.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.065e0

MQ
type: SiteQuality
SIO_000300: 5.864e1

DP
type: SiteQuality
SIO_000300: 3.166189e6

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

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

GenotypeQuality
all individuals: 1929
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variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.399e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.76e-1

QD
type: SiteQuality
SIO_000300: 7.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 8.44e0

DP
type: SiteQuality
SIO_000300: 3.167631e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1628
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 1.503940323647958e-5
allele num: 66492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

QD
type: SiteQuality
SIO_000300: 1.366e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

DP
type: SiteQuality
SIO_000300: 3.167947e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6886
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41047
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.366e1

MQ
type: SiteQuality
SIO_000300: 5.898e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 3.167947e6

GenotypeQuality
all individuals: 1937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6979
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41055
bin: 9.75e1
variant carriers: 73

East Asian
type: Population
allele count: 63
allele frequency: 7.284921369102683e-3
allele num: 8648
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.852602207934004e-4
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

DP
type: SiteQuality
SIO_000300: 3.170595e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeQuality
all individuals: 7106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41034
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1641
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.601e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

FS
type: SiteQuality
SIO_000300: 8.388999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

DP
type: SiteQuality
SIO_000300: 3.168329e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.775e0

QD
type: SiteQuality
SIO_000300: 1.093e1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7163
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41039
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 2102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.516438189979376e-3
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
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: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.163e1

DP
type: SiteQuality
SIO_000300: 3.169942e6

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.464e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

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

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41031
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.049e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.66e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.315e1

MQRankSum
type: SiteQuality
SIO_000300: -1.465e0

DP
type: SiteQuality
SIO_000300: 3.169981e6

GenotypeQuality
all individuals: 41030
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7219
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
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: 16490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.123e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.170365e6

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 1.539e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.81e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

GenotypeQuality
all individuals: 1548
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7211
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41028
bin: 9.75e1
variant carriers: 4

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

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.469010175763182e-4
allele num: 8648
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: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

DP
type: SiteQuality
SIO_000300: 3.170516e6

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

QD
type: SiteQuality
SIO_000300: 1.096e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 6.75e1
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: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 3.170516e6

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

QD
type: SiteQuality
SIO_000300: 1.096e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1549
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41027
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

QD
type: SiteQuality
SIO_000300: 1.467e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.413e0

DP
type: SiteQuality
SIO_000300: 3.170522e6

VQSLOD
type: SiteQuality
SIO_000300: 9.44e-1

GenotypeQuality
all individuals: 1952
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7184
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504233979941145e-5
allele num: 66604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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Latino
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allele frequency: 0.0e0
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (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: 8650
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

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

European (Finnish)
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num of homozygotes: 0

DP
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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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

European (Non-Finnish)
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East Asian
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allele num: 8650
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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
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South Asian
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.003093185981561e-5
allele num: 66598
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

South Asian
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allele num: 16456
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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South Asian
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Other
type: Population
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European (Non-Finnish)
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allele num: 64752
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East Asian
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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QD
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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QD
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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Other
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African
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European (Non-Finnish)
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allele frequency: 1.066162116707211e-3
allele num: 66594
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South Asian
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

South Asian
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allele count: 6
allele frequency: 3.653190452995616e-4
allele num: 16424
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.45e0

BaseQRankSum
type: SiteQuality
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DP
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MQRankSum
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SIO_000300: -3.01e-1

ClippingRankSum
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QD
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InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16422
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.511342126611184e-5
allele num: 66566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.161518e6

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -5.32e0

ClippingRankSum
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SIO_000300: -6.81e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

QD
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FS
type: SiteQuality
SIO_000300: 1.922e0

MQRankSum
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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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 1
allele frequency: 6.093102607847916e-5
allele num: 16412
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: 8650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.585e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 2.834e0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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SIO_000300: 3.160624e6

MQ
type: SiteQuality
SIO_000300: 5.873e1

QD
type: SiteQuality
SIO_000300: 1.469e1

VQSLOD
type: SiteQuality
SIO_000300: -1.399e0

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

African
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allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
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: 0
allele frequency: 0.0e0
allele num: 66558
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: 8650
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.035e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.216e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 3.160363e6

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 121
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.51e-1

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

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.101e0

DP
type: SiteQuality
SIO_000300: 3.159527e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.376e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.829e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509108398965911e-5
allele num: 66532
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 7.57e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

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

European (Non-Finnish)
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allele frequency: 1.540499738115044e-5
allele num: 64914
num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 0.0e0
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African
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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MQ
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele count: 3
allele frequency: 2.617801047120419e-4
allele num: 11460
num of homozygotes: 0

Other
type: Population
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East Asian
type: Population
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allele frequency: 0.0e0
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African
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allele count: 50
allele frequency: 4.871395167575994e-3
allele num: 10264
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66140
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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DP
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MQ
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.712509712509713e-5
allele num: 10296
num of homozygotes: 0

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

Latino
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: 902
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.95e-1

DP
type: SiteQuality
SIO_000300: 1.553152e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10348
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South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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SIO_000300: 1.560718e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 7.152e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 904
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -6.16e-1

FS
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SIO_000300: 6.29e-1

BaseQRankSum
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SIO_000300: 3.6e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

QD
type: SiteQuality
SIO_000300: 1.311e1

FS
type: SiteQuality
SIO_000300: 1.519e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.561659e6

MQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50757
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

VQSLOD
type: SiteQuality
SIO_000300: -1.678e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.561901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.82e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8648
num of homozygotes: 0

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

South Asian
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allele count: 12
allele frequency: 7.278903311901007e-4
allele num: 16486
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
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DP
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VQSLOD
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.55e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

Other
type: Population
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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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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ClippingRankSum
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QD
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DP
type: SiteQuality
SIO_000300: 1.562088e6

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

African
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allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

European (Finnish)
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South Asian
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East Asian
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Latino
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num of homozygotes: 0

Other
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

Other
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allele count: 0
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ClippingRankSum
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SIO_000300: -9.9e-1

ReadPosRankSum
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SIO_000300: 1.44e0

InbreedingCoeff
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DP
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SIO_000300: 1.56699e6

VQSLOD
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FS
type: SiteQuality
SIO_000300: 8.81e-1

MQRankSum
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BaseQRankSum
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SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

QD
type: SiteQuality
SIO_000300: 1.205e1

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.282e0

DP
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MQ
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ClippingRankSum
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VQSLOD
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SIO_000300: -3.9e-3

ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.93e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

QD
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SIO_000300: 1.622e1

MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.0568e1

ClippingRankSum
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DP
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SIO_000300: 1.567556e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.068697657482704e-5
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: 9.1e-3

ReadPosRankSum
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 1.491e0

DP
type: SiteQuality
SIO_000300: 1.56693e6

QD
type: SiteQuality
SIO_000300: 8.81e0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

South Asian
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allele frequency: 3.643429681807141e-4
allele num: 16468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

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

African
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allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503940323647958e-5
allele num: 66492
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
type: Population
allele count: 1
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allele num: 66470
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Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.904e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

African
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allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.9e1

DP
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QD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 8.35e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66302
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: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.637625289128758e-5
allele num: 10376
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
allele num: 11458
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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DP
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VQSLOD
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QD
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 1.7e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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allele frequency: 9.650646593321752e-5
allele num: 10362
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 count: 6
allele frequency: 9.102217907096695e-5
allele num: 65918
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East Asian
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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FS
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DP
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MQ
type: SiteQuality
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.517773123273533e-5
allele num: 65886
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
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Other
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

VQSLOD
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DP
type: SiteQuality
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 3.036560184622859e-5
allele num: 65864
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East Asian
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African
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South Asian
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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FS
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MQRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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Other
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Latino
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East Asian
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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DP
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QD
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Other
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African
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European (Finnish)
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Latino
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East Asian
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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African
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Latino
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South Asian
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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SIO_000300: 1.364e1

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

DP
type: SiteQuality
SIO_000300: 1.443683e6

GenotypeQuality
all individuals: 339
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5061
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1578
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4327
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3912
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.152386356471849e-5
allele num: 31722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3272
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.69e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.74e0

DP
type: SiteQuality
SIO_000300: 1.439031e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

MQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.042e1

QD
type: SiteQuality
SIO_000300: 4.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

GenotypeQuality
all individuals: 4440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 926
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2539
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31236
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3934
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2022
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.428387760349704e-5
allele num: 15556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

DP
type: SiteQuality
SIO_000300: 1.395044e6

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

GenotypeQuality
all individuals: 285
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.75e1
variant carriers: 0