7-97488121-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488121
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488121
    reference: chr 7
allele count: 1
allele frequency: 8.445803280349994e-6
allele num: 118402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+45A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+45A>T
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3540
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20660
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1757
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-97488131-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488131
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488131
    reference: chr 7
allele count: 12
allele frequency: 1.026149715243454e-4
allele num: 116942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+35T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+35T>C
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5639
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

7-97488136-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488136
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488136
    reference: chr 7
allele count: 1
allele frequency: 8.696710903936131e-6
allele num: 114986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+30T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+30T>A
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-97488145-GGTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488145
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488142
    reference: chr 7
allele count: 1
allele frequency: 9.5580363970026e-6
allele num: 104624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+18_775+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+18_775+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+18_526+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+18_775+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+18_526+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+18_712+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+18_775+20delAAC
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+18_712+20delAAC
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: GGTT
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS

7-97488146-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488146
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488147
    reference: chr 7
allele count: 39473
allele frequency: 3.280722751375522e-1
allele num: 120318
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+19dupA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+19dupA
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 1786
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 7.25e1
  variant carriers: 2284
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 898
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 4.25e1
  variant carriers: 1365
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 1163
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 393
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 5.25e1
  variant carriers: 2210
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 6.25e1
  variant carriers: 2472
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 3.25e1
  variant carriers: 919
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 4.75e1
  variant carriers: 1785
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 3.75e1
  variant carriers: 1087
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 2.25e1
  variant carriers: 1122
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 1110
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 5.75e1
  variant carriers: 2400
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 9.75e1
  variant carriers: 5464
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 6.75e1
  variant carriers: 2371
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.75e1
  variant carriers: 2061
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.75e1
  variant carriers: 1502
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 7.25e1
  variant carriers: 115
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 6.25e1
  variant carriers: 83
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 8.25e1
  variant carriers: 119
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 10
num of homozygotes: 7111
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-97488146-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488146
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488148
    reference: chr 7
allele count: 1247
allele frequency: 1.036420153260526e-2
allele num: 120318
alternate allele: GTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+18_775+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+18_526+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+18_712+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+18_775+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+18_712+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+18_775+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+18_526+19dupAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+18_775+19dupAA
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 5.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 7.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 9.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 3.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 6.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 4.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 5.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 6.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 4.75e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 26
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

7-97488146-G-GTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488146
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488149
    reference: chr 7
allele count: 4
allele frequency: 3.324523346465201e-5
allele num: 120318
alternate allele: GTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+17_712+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+17_526+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+17_775+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+17_775+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+17_775+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+17_526+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+17_775+19dupAAA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+17_712+19dupAAA
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

7-97488146-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488146
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488145
    reference: chr 7
allele count: 6
allele frequency: 4.986785019697801e-5
allele num: 120318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+19delA
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+19delA
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43350
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: GT
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

7-97488153-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488153
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488153
    reference: chr 7
allele count: 7
allele frequency: 5.80508193458502e-5
allele num: 120584
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+13A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+13A>T
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1869
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3554
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27660
  bin: 9.75e1
  variant carriers: 7
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

7-97488153-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488153
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488152
    reference: chr 7
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.526+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.712+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.775+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.775+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.775+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.526+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.775+12delT
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.712+12delT
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27660
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: TA
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/7-97488183-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488183
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488183
    reference: chr 7
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.758T>G
  hgvsp: ENSP00000377845.3:p.Ile253Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.758T>G
  hgvsp: ENSP00000175506.4:p.Ile253Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.509T>G
  hgvsp: ENSP00000414379.1:p.Ile170Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.695T>G
  hgvsp: ENSP00000414901.1:p.Ile232Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.758T>G
  hgvsp: ENSP00000377846.3:p.Ile253Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.695T>G
  hgvsp: ENSP00000406994.1:p.Ile232Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.509T>G
  hgvsp: ENSP00000408472.1:p.Ile170Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.758T>G
  hgvsp: ENSP00000401651.1:p.Ile253Ser
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3563
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13668
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile253Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

7-97488185-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488185
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488182
    reference: chr 7
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.690_692delAAG
  hgvsp: ENSP00000406994.1:p.Arg231del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.504_506delAAG
  hgvsp: ENSP00000408472.1:p.Arg169del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.753_755delAAG
  hgvsp: ENSP00000401651.1:p.Arg252del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.753_755delAAG
  hgvsp: ENSP00000377846.3:p.Arg252del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.504_506delAAG
  hgvsp: ENSP00000414379.1:p.Arg169del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.690_692delAAG
  hgvsp: ENSP00000414901.1:p.Arg231del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.753_755delAAG
  hgvsp: ENSP00000377845.3:p.Arg252del
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.753_755delAAG
  hgvsp: ENSP00000175506.4:p.Arg252del
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13654
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg252del
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: CCTT
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

7-97488195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488195
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488195
    reference: chr 7
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.746C>T
  hgvsp: ENSP00000377846.3:p.Thr249Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.746C>T
  hgvsp: ENSP00000377845.3:p.Thr249Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.746C>T
  hgvsp: ENSP00000175506.4:p.Thr249Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.746C>T
  hgvsp: ENSP00000401651.1:p.Thr249Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.497C>T
  hgvsp: ENSP00000408472.1:p.Thr166Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.683C>T
  hgvsp: ENSP00000414901.1:p.Thr228Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.683C>T
  hgvsp: ENSP00000406994.1:p.Thr228Ile
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.497C>T
  hgvsp: ENSP00000414379.1:p.Thr166Ile
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3561
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr249Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

7-97488199-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488199
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488199
    reference: chr 7
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.679A>C
  hgvsp: ENSP00000406994.1:p.Met227Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.742A>C
  hgvsp: ENSP00000175506.4:p.Met248Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.742A>C
  hgvsp: ENSP00000377845.3:p.Met248Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.493A>C
  hgvsp: ENSP00000408472.1:p.Met165Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.679A>C
  hgvsp: ENSP00000414901.1:p.Met227Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.742A>C
  hgvsp: ENSP00000401651.1:p.Met248Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.742A>C
  hgvsp: ENSP00000377846.3:p.Met248Leu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.493A>C
  hgvsp: ENSP00000414379.1:p.Met165Leu
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met248Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum

7-97488205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488205
    reference: chr 7
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.736C>T
  hgvsp: ENSP00000377846.3:p.Arg246Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.736C>T
  hgvsp: ENSP00000377845.3:p.Arg246Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.673C>T
  hgvsp: ENSP00000414901.1:p.Arg225Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.487C>T
  hgvsp: ENSP00000414379.1:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.673C>T
  hgvsp: ENSP00000406994.1:p.Arg225Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.487C>T
  hgvsp: ENSP00000408472.1:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.736C>T
  hgvsp: ENSP00000401651.1:p.Arg246Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.736C>T
  hgvsp: ENSP00000175506.4:p.Arg246Cys
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4553
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg246Cys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

7-97488208-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488208
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488207
    reference: chr 7
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.483delG
  hgvsp: ENSP00000414379.1:p.Lys162AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.669delG
  hgvsp: ENSP00000414901.1:p.Lys224AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.732delG
  hgvsp: ENSP00000377846.3:p.Lys245AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.732delG
  hgvsp: ENSP00000175506.4:p.Lys245AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.732delG
  hgvsp: ENSP00000377845.3:p.Lys245AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.669delG
  hgvsp: ENSP00000406994.1:p.Lys224AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.732delG
  hgvsp: ENSP00000401651.1:p.Lys245AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.483delG
  hgvsp: ENSP00000408472.1:p.Lys162AsnfsTer3
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27644
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys245AsnfsTer3
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: TC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

7-97488210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488210
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488210
    reference: chr 7
allele count: 2
allele frequency: 1.653411815280832e-5
allele num: 120962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.731A>G
  hgvsp: ENSP00000401651.1:p.Lys244Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.482A>G
  hgvsp: ENSP00000408472.1:p.Lys161Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.668A>G
  hgvsp: ENSP00000406994.1:p.Lys223Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.731A>G
  hgvsp: ENSP00000175506.4:p.Lys244Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.731A>G
  hgvsp: ENSP00000377846.3:p.Lys244Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.482A>G
  hgvsp: ENSP00000414379.1:p.Lys161Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.731A>G
  hgvsp: ENSP00000377845.3:p.Lys244Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.668A>G
  hgvsp: ENSP00000414901.1:p.Lys223Arg
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys244Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

7-97488213-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488213
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488213
    reference: chr 7
allele count: 1
allele frequency: 8.267059076404159e-6
allele num: 120962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.665T>C
  hgvsp: ENSP00000406994.1:p.Val222Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.479T>C
  hgvsp: ENSP00000408472.1:p.Val160Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.728T>C
  hgvsp: ENSP00000377846.3:p.Val243Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.728T>C
  hgvsp: ENSP00000175506.4:p.Val243Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.728T>C
  hgvsp: ENSP00000377845.3:p.Val243Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.479T>C
  hgvsp: ENSP00000414379.1:p.Val160Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.665T>C
  hgvsp: ENSP00000414901.1:p.Val222Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.728T>C
  hgvsp: ENSP00000401651.1:p.Val243Ala
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8441
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val243Ala
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-97488249-A-ACAGTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488249
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488254
    reference: chr 7
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: ACAGTT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.687_691dupAACTG
  hgvsp: ENSP00000377845.3:p.Val231GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.624_628dupAACTG
  hgvsp: ENSP00000414901.1:p.Val210GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.687_691dupAACTG
  hgvsp: ENSP00000175506.4:p.Val231GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.624_628dupAACTG
  hgvsp: ENSP00000406994.1:p.Val210GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.438_442dupAACTG
  hgvsp: ENSP00000408472.1:p.Val148GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.438_442dupAACTG
  hgvsp: ENSP00000414379.1:p.Val148GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.687_691dupAACTG
  hgvsp: ENSP00000377846.3:p.Val231GlufsTer3
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.687_691dupAACTG
  hgvsp: ENSP00000401651.1:p.Val231GlufsTer3
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8432
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27642
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val231GlufsTer3
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

7-97488253-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488253
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488253
    reference: chr 7
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.625A>G
  hgvsp: ENSP00000414901.1:p.Thr209Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.688A>G
  hgvsp: ENSP00000401651.1:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.625A>G
  hgvsp: ENSP00000406994.1:p.Thr209Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.688A>G
  hgvsp: ENSP00000377846.3:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.688A>G
  hgvsp: ENSP00000175506.4:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.439A>G
  hgvsp: ENSP00000408472.1:p.Thr147Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.439A>G
  hgvsp: ENSP00000414379.1:p.Thr147Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.688A>G
  hgvsp: ENSP00000377845.3:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27641
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4530
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr230Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

7-97488271-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488271
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488271
    reference: chr 7
allele count: 1
allele frequency: 8.306475728477921e-6
allele num: 120388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-4A>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-4A>T
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27636
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: c.674-4A>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-97488273-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488273
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488273
    reference: chr 7
allele count: 5
allele frequency: 4.154618273673015e-5
allele num: 120348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-6T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-6T>G
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
hgvs: c.674-6T>G
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

7-97488275-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488275
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488275
    reference: chr 7
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-8G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-8G>A
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
hgvs: c.674-8G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

7-97488283-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488283
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488283
    reference: chr 7
allele count: 2
allele frequency: 1.664918502239315e-5
allele num: 120126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-16A>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-16A>C
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4340
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

7-97488292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488292
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488292
    reference: chr 7
allele count: 433
allele frequency: 3.610860935988525e-3
allele num: 119916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-25G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-25G>A
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 3.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 2.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 2.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 27866
  bin: 9.75e1
  variant carriers: 423
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3485
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 5
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-97488293-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488293
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488293
    reference: chr 7
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-26T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-26T>C
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7165
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27587
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

7-97488314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488314
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488314
    reference: chr 7
allele count: 1
allele frequency: 8.385603595746822e-6
allele num: 119252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.611-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.674-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.674-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.611-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.674-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.425-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.674-47C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.425-47C>T
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3347
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-97488474-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488474
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488474
    reference: chr 7
allele count: 3
allele frequency: 2.610239097901368e-5
allele num: 114932
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+51T>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+51T>G
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9225
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3470
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD

7-97488474-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488474
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488474
    reference: chr 7
allele count: 132
allele frequency: 1.148505203076602e-3
allele num: 114932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+51T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+51T>A
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9225
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3530
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-97488475-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488475
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488475
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 114980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+50A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+50A>G
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

7-97488480-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488480
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488480
    reference: chr 7
allele count: 1
allele frequency: 8.658758334054896e-6
allele num: 115490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+45A>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+45A>G
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

7-97488483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488483
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488483
    reference: chr 7
allele count: 6
allele frequency: 5.193366340061628e-5
allele num: 115532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+42G>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+42G>A
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6924
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3691
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-97488491-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488491
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488491
    reference: chr 7
allele count: 1
allele frequency: 8.612819320276298e-6
allele num: 116106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+34T>A
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+34T>A
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3714
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

7-97488492-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488492
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488492
    reference: chr 7
allele count: 1
allele frequency: 8.607777988190129e-6
allele num: 116174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+33T>C
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+33T>C
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3731
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3723
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7460
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

7-97488498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488498
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488498
    reference: chr 7
allele count: 1
allele frequency: 8.575152637716951e-6
allele num: 116616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+27C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+27C>T
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

7-97488506-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488506
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488506
    reference: chr 7
allele count: 12
allele frequency: 1.023925731253626e-4
allele num: 117196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+19C>G
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+19C>G
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3982
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28107
  bin: 9.75e1
  variant carriers: 12
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

7-97488509-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488509
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488509
    reference: chr 7
allele count: 1
allele frequency: 8.512666848270226e-6
allele num: 117472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.673+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.424+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.610+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.673+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.424+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.610+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.673+16C>T
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.673+16C>T
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-97488528-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488528
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488528
    reference: chr 7
allele count: 2
allele frequency: 1.67521023888498e-5
allele num: 119388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.670C>G
  hgvsp: ENSP00000401651.1:p.Pro224Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.421C>G
  hgvsp: ENSP00000414379.1:p.Pro141Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.670C>G
  hgvsp: ENSP00000377846.3:p.Pro224Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.670C>G
  hgvsp: ENSP00000175506.4:p.Pro224Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.607C>G
  hgvsp: ENSP00000414901.1:p.Pro203Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.607C>G
  hgvsp: ENSP00000406994.1:p.Pro203Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.670C>G
  hgvsp: ENSP00000377845.3:p.Pro224Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.421C>G
  hgvsp: ENSP00000408472.1:p.Pro141Ala
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2491
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro224Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

7-97488530-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488530
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488528
    reference: chr 7
allele count: 1
allele frequency: 8.363861427543869e-6
allele num: 119562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.417_418delCT
  hgvsp: ENSP00000414379.1:p.Phe140SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.603_604delCT
  hgvsp: ENSP00000406994.1:p.Phe202SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.603_604delCT
  hgvsp: ENSP00000414901.1:p.Phe202SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.666_667delCT
  hgvsp: ENSP00000401651.1:p.Phe223SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.417_418delCT
  hgvsp: ENSP00000408472.1:p.Phe140SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.666_667delCT
  hgvsp: ENSP00000175506.4:p.Phe223SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.666_667delCT
  hgvsp: ENSP00000377845.3:p.Phe223SerfsTer4
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.666_667delCT
  hgvsp: ENSP00000377846.3:p.Phe223SerfsTer4
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe223SerfsTer4
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: AAG
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-97488544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488544
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488544
    reference: chr 7
allele count: 3
allele frequency: 2.491404653943893e-5
allele num: 120414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.654T>C
  hgvsp: ENST00000394309.3:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.405T>C
  hgvsp: ENST00000455086.1:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.591T>C
  hgvsp: ENST00000422745.1:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.654T>C
  hgvsp: ENST00000454046.1:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.591T>C
  hgvsp: ENST00000444334.1:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.654T>C
  hgvsp: ENST00000394308.3:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.405T>C
  hgvsp: ENST00000437628.1:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.654T>C
  hgvsp: ENST00000175506.4:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28169
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn218Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

7-97488551-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488551
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488551
    reference: chr 7
allele count: 2
allele frequency: 1.656314699792961e-5
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.584A>G
  hgvsp: ENSP00000414901.1:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.647A>G
  hgvsp: ENSP00000401651.1:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.647A>G
  hgvsp: ENSP00000175506.4:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.584A>G
  hgvsp: ENSP00000406994.1:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.398A>G
  hgvsp: ENSP00000408472.1:p.Tyr133Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.398A>G
  hgvsp: ENSP00000414379.1:p.Tyr133Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.647A>G
  hgvsp: ENSP00000377846.3:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.647A>G
  hgvsp: ENSP00000377845.3:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr216Cys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

7-97488562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488562
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488562
    reference: chr 7
allele count: 1
allele frequency: 8.262004692818665e-6
allele num: 121036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.387G>A
  hgvsp: ENST00000455086.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.636G>A
  hgvsp: ENST00000442734.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.636G>A
  hgvsp: ENST00000175506.4:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.636G>A
  hgvsp: ENST00000394308.3:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.573G>A
  hgvsp: ENST00000422745.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.636G>A
  hgvsp: ENST00000454046.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.387G>A
  hgvsp: ENST00000437628.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.573G>A
  hgvsp: ENST00000444334.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.636G>A
  hgvsp: ENST00000394309.3:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4104
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu212Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

7-97488569-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488569
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488569
    reference: chr 7
allele count: 96470
allele frequency: 7.94776734223101e-1
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.380T>A
  hgvsp: ENSP00000408472.1:p.Val127Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.380T>A
  hgvsp: ENSP00000414379.1:p.Val127Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.629T>A
  hgvsp: ENSP00000377846.3:p.Val210Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.629T>A
  hgvsp: ENSP00000377845.3:p.Val210Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.629T>A
  hgvsp: ENSP00000175506.4:p.Val210Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.629T>A
  hgvsp: ENSP00000401651.1:p.Val210Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.566T>A
  hgvsp: ENSP00000414901.1:p.Val189Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.629T>A
  hgvsp: ENSP00000400422.1:p.Val210Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.566T>A
  hgvsp: ENSP00000406994.1:p.Val189Glu
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 6.75e1
  variant carriers: 2076
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 9.25e1
  variant carriers: 3664
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.75e1
  variant carriers: 921
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 7.25e1
  variant carriers: 2496
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 1090
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.75e1
  variant carriers: 453
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.25e1
  variant carriers: 702
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 7.75e1
  variant carriers: 2899
genotype depth: GenotypeDepth
  all individuals: 30540
  bin: 9.75e1
  variant carriers: 30530
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 8.75e1
  variant carriers: 3585
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 1190
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.25e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.25e1
  variant carriers: 3263
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 1336
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 6.25e1
  variant carriers: 1744
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 1428
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 25
hgvs: p.Val210Glu
num of homozygotes: 38723
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

7-97488571-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488571
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488571
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.627T>A
  hgvsp: ENSP00000175506.4:p.Asp209Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.378T>A
  hgvsp: ENSP00000414379.1:p.Asp126Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.564T>A
  hgvsp: ENSP00000406994.1:p.Asp188Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.564T>A
  hgvsp: ENSP00000414901.1:p.Asp188Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.627T>A
  hgvsp: ENSP00000401651.1:p.Asp209Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.627T>A
  hgvsp: ENSP00000377845.3:p.Asp209Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.378T>A
  hgvsp: ENSP00000408472.1:p.Asp126Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.627T>A
  hgvsp: ENSP00000400422.1:p.Asp209Glu
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.627T>A
  hgvsp: ENSP00000377846.3:p.Asp209Glu
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19380
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp209Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-97488574-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488574
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488574
    reference: chr 7
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.624G>T
  hgvsp: ENST00000454046.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.624G>T
  hgvsp: ENST00000394308.3:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.375G>T
  hgvsp: ENST00000437628.1:c.375G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.561G>T
  hgvsp: ENST00000422745.1:c.561G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.624G>T
  hgvsp: ENST00000442734.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.624G>T
  hgvsp: ENST00000175506.4:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.375G>T
  hgvsp: ENST00000455086.1:c.375G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.624G>T
  hgvsp: ENST00000394309.3:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.561G>T
  hgvsp: ENST00000444334.1:c.561G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14419
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg208Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-97488575-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488575
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488575
    reference: chr 7
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.623G>A
  hgvsp: ENSP00000401651.1:p.Arg208Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.374G>A
  hgvsp: ENSP00000408472.1:p.Arg125Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.374G>A
  hgvsp: ENSP00000414379.1:p.Arg125Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.560G>A
  hgvsp: ENSP00000414901.1:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.623G>A
  hgvsp: ENSP00000400422.1:p.Arg208Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.623G>A
  hgvsp: ENSP00000377845.3:p.Arg208Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.560G>A
  hgvsp: ENSP00000406994.1:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.623G>A
  hgvsp: ENSP00000377846.3:p.Arg208Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.623G>A
  hgvsp: ENSP00000175506.4:p.Arg208Gln
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3789
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg208Gln
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-97488578-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488578
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488578
    reference: chr 7
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.557G>C
  hgvsp: ENSP00000414901.1:p.Cys186Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.620G>C
  hgvsp: ENSP00000401651.1:p.Cys207Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.557G>C
  hgvsp: ENSP00000406994.1:p.Cys186Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.620G>C
  hgvsp: ENSP00000400422.1:p.Cys207Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.620G>C
  hgvsp: ENSP00000175506.4:p.Cys207Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.371G>C
  hgvsp: ENSP00000408472.1:p.Cys124Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.371G>C
  hgvsp: ENSP00000414379.1:p.Cys124Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.620G>C
  hgvsp: ENSP00000377846.3:p.Cys207Ser
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.620G>C
  hgvsp: ENSP00000377845.3:p.Cys207Ser
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys207Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

7-97488580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488580
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488580
    reference: chr 7
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.369C>T
  hgvsp: ENST00000455086.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.618C>T
  hgvsp: ENST00000454046.1:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.618C>T
  hgvsp: ENST00000394308.3:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.555C>T
  hgvsp: ENST00000444334.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.618C>T
  hgvsp: ENST00000394309.3:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.369C>T
  hgvsp: ENST00000437628.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.555C>T
  hgvsp: ENST00000422745.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.618C>T
  hgvsp: ENST00000442734.1:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.618C>T
  hgvsp: ENST00000175506.4:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His206His
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

7-97488587-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488587
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488587
    reference: chr 7
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.611A>G
  hgvsp: ENSP00000377846.3:p.Tyr204Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.611A>G
  hgvsp: ENSP00000400422.1:p.Tyr204Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.362A>G
  hgvsp: ENSP00000408472.1:p.Tyr121Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.548A>G
  hgvsp: ENSP00000414901.1:p.Tyr183Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.611A>G
  hgvsp: ENSP00000401651.1:p.Tyr204Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.548A>G
  hgvsp: ENSP00000406994.1:p.Tyr183Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.611A>G
  hgvsp: ENSP00000175506.4:p.Tyr204Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.611A>G
  hgvsp: ENSP00000377845.3:p.Tyr204Cys
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.362A>G
  hgvsp: ENSP00000414379.1:p.Tyr121Cys
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr204Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

7-97488601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488601
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488601
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.597G>A
  hgvsp: ENST00000394308.3:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.348G>A
  hgvsp: ENST00000437628.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.597G>A
  hgvsp: ENST00000175506.4:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.348G>A
  hgvsp: ENST00000455086.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.597G>A
  hgvsp: ENST00000454046.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.534G>A
  hgvsp: ENST00000422745.1:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.597G>A
  hgvsp: ENST00000442734.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.597G>A
  hgvsp: ENST00000394309.3:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.534G>A
  hgvsp: ENST00000444334.1:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val199Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

7-97488604-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488604
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488604
    reference: chr 7
allele count: 7
allele frequency: 5.76672762921589e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.594C>T
  hgvsp: ENST00000442734.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.531C>T
  hgvsp: ENST00000422745.1:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.594C>T
  hgvsp: ENST00000394308.3:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.594C>T
  hgvsp: ENST00000394309.3:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.531C>T
  hgvsp: ENST00000444334.1:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.594C>T
  hgvsp: ENST00000175506.4:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.345C>T
  hgvsp: ENST00000455086.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.345C>T
  hgvsp: ENST00000437628.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.594C>T
  hgvsp: ENST00000454046.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3133
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser198Ser
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

7-97488607-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488607
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488607
    reference: chr 7
allele count: 68
allele frequency: 5.601963982666864e-4
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.591A>C
  hgvsp: ENST00000442734.1:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.528A>C
  hgvsp: ENST00000444334.1:c.528A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.342A>C
  hgvsp: ENST00000437628.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.342A>C
  hgvsp: ENST00000455086.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.591A>C
  hgvsp: ENST00000175506.4:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.591A>C
  hgvsp: ENST00000394308.3:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.528A>C
  hgvsp: ENST00000422745.1:c.528A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.591A>C
  hgvsp: ENST00000394309.3:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.591A>C
  hgvsp: ENST00000454046.1:c.591A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20151
  bin: 9.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala197Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

7-97488631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488631
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488631
    reference: chr 7
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.504T>C
  hgvsp: ENST00000422745.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.567T>C
  hgvsp: ENST00000454046.1:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.504T>C
  hgvsp: ENST00000444334.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.318T>C
  hgvsp: ENST00000455086.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.318T>C
  hgvsp: ENST00000437628.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.567T>C
  hgvsp: ENST00000175506.4:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.567T>C
  hgvsp: ENST00000442734.1:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.567T>C
  hgvsp: ENST00000394308.3:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.567T>C
  hgvsp: ENST00000394309.3:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp189Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP

7-97488632-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488632
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488632
    reference: chr 7
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.317A>G
  hgvsp: ENSP00000414379.1:p.Asp106Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.566A>G
  hgvsp: ENSP00000401651.1:p.Asp189Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.503A>G
  hgvsp: ENSP00000414901.1:p.Asp168Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.566A>G
  hgvsp: ENSP00000400422.1:p.Asp189Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.566A>G
  hgvsp: ENSP00000175506.4:p.Asp189Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.503A>G
  hgvsp: ENSP00000406994.1:p.Asp168Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.317A>G
  hgvsp: ENSP00000408472.1:p.Asp106Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.566A>G
  hgvsp: ENSP00000377846.3:p.Asp189Gly
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.566A>G
  hgvsp: ENSP00000377845.3:p.Asp189Gly
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20104
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp189Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

7-97488647-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488647
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488647
    reference: chr 7
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.302A>G
  hgvsp: ENSP00000414379.1:p.His101Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.488A>G
  hgvsp: ENSP00000406994.1:p.His163Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.488A>G
  hgvsp: ENSP00000414901.1:p.His163Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.302A>G
  hgvsp: ENSP00000408472.1:p.His101Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.551A>G
  hgvsp: ENSP00000377845.3:p.His184Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.551A>G
  hgvsp: ENSP00000175506.4:p.His184Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.551A>G
  hgvsp: ENSP00000400422.1:p.His184Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.551A>G
  hgvsp: ENSP00000377846.3:p.His184Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.551A>G
  hgvsp: ENSP00000401651.1:p.His184Arg
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His184Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

7-97488655-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488655
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488655
    reference: chr 7
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.480T>C
  hgvsp: ENST00000444334.1:c.480T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.543T>C
  hgvsp: ENST00000175506.4:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.480T>C
  hgvsp: ENST00000422745.1:c.480T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.543T>C
  hgvsp: ENST00000394308.3:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.543T>C
  hgvsp: ENST00000442734.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.543T>C
  hgvsp: ENST00000454046.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.294T>C
  hgvsp: ENST00000437628.1:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.294T>C
  hgvsp: ENST00000455086.1:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.543T>C
  hgvsp: ENST00000394309.3:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu181Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

7-97488663-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488663
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488663
    reference: chr 7
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.535C>G
  hgvsp: ENSP00000401651.1:p.Pro179Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.535C>G
  hgvsp: ENSP00000400422.1:p.Pro179Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.472C>G
  hgvsp: ENSP00000406994.1:p.Pro158Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.535C>G
  hgvsp: ENSP00000377845.3:p.Pro179Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.472C>G
  hgvsp: ENSP00000414901.1:p.Pro158Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.535C>G
  hgvsp: ENSP00000377846.3:p.Pro179Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.286C>G
  hgvsp: ENSP00000414379.1:p.Pro96Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.286C>G
  hgvsp: ENSP00000408472.1:p.Pro96Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.535C>G
  hgvsp: ENSP00000175506.4:p.Pro179Ala
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3432
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro179Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

7-97488670-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488670
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488670
    reference: chr 7
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.465A>C
  hgvsp: ENSP00000406994.1:p.Lys155Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.528A>C
  hgvsp: ENSP00000175506.4:p.Lys176Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.279A>C
  hgvsp: ENSP00000414379.1:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.528A>C
  hgvsp: ENSP00000401651.1:p.Lys176Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.465A>C
  hgvsp: ENSP00000414901.1:p.Lys155Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.528A>C
  hgvsp: ENSP00000400422.1:p.Lys176Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.528A>C
  hgvsp: ENSP00000377845.3:p.Lys176Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.528A>C
  hgvsp: ENSP00000377846.3:p.Lys176Asn
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.279A>C
  hgvsp: ENSP00000408472.1:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20086
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys176Asn
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-97488673-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488673
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488673
    reference: chr 7
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.462A>T
  hgvsp: ENSP00000414901.1:p.Leu154Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.276A>T
  hgvsp: ENSP00000408472.1:p.Leu92Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.525A>T
  hgvsp: ENSP00000400422.1:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.462A>T
  hgvsp: ENSP00000406994.1:p.Leu154Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.525A>T
  hgvsp: ENSP00000175506.4:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.525A>T
  hgvsp: ENSP00000401651.1:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.276A>T
  hgvsp: ENSP00000414379.1:p.Leu92Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.525A>T
  hgvsp: ENSP00000377846.3:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.525A>T
  hgvsp: ENSP00000377845.3:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu175Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/7-97488678-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488678
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488678
    reference: chr 7
allele count: 3
allele frequency: 2.49708673214583e-5
allele num: 120140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.457T>G
  hgvsp: ENSP00000414901.1:p.Phe153Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.520T>G
  hgvsp: ENSP00000400422.1:p.Phe174Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.271T>G
  hgvsp: ENSP00000408472.1:p.Phe91Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.520T>G
  hgvsp: ENSP00000401651.1:p.Phe174Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.520T>G
  hgvsp: ENSP00000175506.4:p.Phe174Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.520T>G
  hgvsp: ENSP00000377846.3:p.Phe174Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.520T>G
  hgvsp: ENSP00000377845.3:p.Phe174Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.457T>G
  hgvsp: ENSP00000406994.1:p.Phe153Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.271T>G
  hgvsp: ENSP00000414379.1:p.Phe91Val
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe174Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

7-97488685-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488685
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488685
    reference: chr 7
allele count: 2
allele frequency: 1.671318503167149e-5
allele num: 119666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.450G>A
  hgvsp: ENST00000444334.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.264G>A
  hgvsp: ENST00000455086.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.513G>A
  hgvsp: ENST00000442734.1:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.513G>A
  hgvsp: ENST00000175506.4:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.264G>A
  hgvsp: ENST00000437628.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.513G>A
  hgvsp: ENST00000394309.3:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.450G>A
  hgvsp: ENST00000422745.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.513G>A
  hgvsp: ENST00000394308.3:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.513G>A
  hgvsp: ENST00000454046.1:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala171Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

7-97488686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488686
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488686
    reference: chr 7
allele count: 3
allele frequency: 2.507396820620831e-5
allele num: 119646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.263C>T
  hgvsp: ENSP00000408472.1:p.Ala88Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.512C>T
  hgvsp: ENSP00000401651.1:p.Ala171Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.512C>T
  hgvsp: ENSP00000377846.3:p.Ala171Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.449C>T
  hgvsp: ENSP00000406994.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.512C>T
  hgvsp: ENSP00000175506.4:p.Ala171Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.449C>T
  hgvsp: ENSP00000414901.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.512C>T
  hgvsp: ENSP00000400422.1:p.Ala171Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.263C>T
  hgvsp: ENSP00000414379.1:p.Ala88Val
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.512C>T
  hgvsp: ENSP00000377845.3:p.Ala171Val
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala171Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

7-97488687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488687
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488687
    reference: chr 7
allele count: 5
allele frequency: 4.183680299886204e-5
allele num: 119512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.262G>A
  hgvsp: ENSP00000414379.1:p.Ala88Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.511G>A
  hgvsp: ENSP00000401651.1:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.511G>A
  hgvsp: ENSP00000400422.1:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.511G>A
  hgvsp: ENSP00000377846.3:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.448G>A
  hgvsp: ENSP00000414901.1:p.Ala150Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.448G>A
  hgvsp: ENSP00000406994.1:p.Ala150Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.262G>A
  hgvsp: ENSP00000408472.1:p.Ala88Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.511G>A
  hgvsp: ENSP00000377845.3:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.511G>A
  hgvsp: ENSP00000175506.4:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13084
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3122
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala171Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

7-97488688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488688
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488688
    reference: chr 7
allele count: 5
allele frequency: 4.183330265557805e-5
allele num: 119522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.510C>T
  hgvsp: ENST00000394309.3:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.261C>T
  hgvsp: ENST00000437628.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.510C>T
  hgvsp: ENST00000394308.3:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.447C>T
  hgvsp: ENST00000422745.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.510C>T
  hgvsp: ENST00000454046.1:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.510C>T
  hgvsp: ENST00000442734.1:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.510C>T
  hgvsp: ENST00000175506.4:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.261C>T
  hgvsp: ENST00000455086.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.447C>T
  hgvsp: ENST00000444334.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20071
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser170Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

7-97488691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488691
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488691
    reference: chr 7
allele count: 1
allele frequency: 8.386025527061704e-6
allele num: 119246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.507C>T
  hgvsp: ENST00000394308.3:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.507C>T
  hgvsp: ENST00000442734.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.507C>T
  hgvsp: ENST00000175506.4:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.507C>T
  hgvsp: ENST00000454046.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.258C>T
  hgvsp: ENST00000437628.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.444C>T
  hgvsp: ENST00000422745.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.258C>T
  hgvsp: ENST00000455086.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.444C>T
  hgvsp: ENST00000444334.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.507C>T
  hgvsp: ENST00000394309.3:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3688
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His169His
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-97488691-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488691
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488691
    reference: chr 7
allele count: 15
allele frequency: 1.257903829059256e-4
allele num: 119246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.258C>G
  hgvsp: ENSP00000414379.1:p.His86Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.507C>G
  hgvsp: ENSP00000175506.4:p.His169Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.507C>G
  hgvsp: ENSP00000400422.1:p.His169Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.444C>G
  hgvsp: ENSP00000406994.1:p.His148Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.507C>G
  hgvsp: ENSP00000377846.3:p.His169Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.258C>G
  hgvsp: ENSP00000408472.1:p.His86Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.507C>G
  hgvsp: ENSP00000377845.3:p.His169Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.444C>G
  hgvsp: ENSP00000414901.1:p.His148Gln
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.507C>G
  hgvsp: ENSP00000401651.1:p.His169Gln
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His169Gln
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

7-97488692-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488692
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488692
    reference: chr 7
allele count: 1
allele frequency: 8.386588168201411e-6
allele num: 119238
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.506A>G
  hgvsp: ENSP00000175506.4:p.His169Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.443A>G
  hgvsp: ENSP00000406994.1:p.His148Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.506A>G
  hgvsp: ENSP00000401651.1:p.His169Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.257A>G
  hgvsp: ENSP00000408472.1:p.His86Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.506A>G
  hgvsp: ENSP00000377846.3:p.His169Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.443A>G
  hgvsp: ENSP00000414901.1:p.His148Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.257A>G
  hgvsp: ENSP00000414379.1:p.His86Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.506A>G
  hgvsp: ENSP00000377845.3:p.His169Arg
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.506A>G
  hgvsp: ENSP00000400422.1:p.His169Arg
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3122
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His169Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

7-97488699-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488699
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488699
    reference: chr 7
allele count: 1
allele frequency: 8.422329279385507e-6
allele num: 118732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.499T>C
  hgvsp: ENST00000394308.3:c.499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.499T>C
  hgvsp: ENST00000442734.1:c.499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.436T>C
  hgvsp: ENST00000422745.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.250T>C
  hgvsp: ENST00000455086.1:c.250T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.250T>C
  hgvsp: ENST00000437628.1:c.250T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.499T>C
  hgvsp: ENST00000454046.1:c.499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.499T>C
  hgvsp: ENST00000175506.4:c.499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.436T>C
  hgvsp: ENST00000444334.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.499T>C
  hgvsp: ENST00000394309.3:c.499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu167Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

7-97488704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488704
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488704
    reference: chr 7
allele count: 2
allele frequency: 1.688561683158286e-5
allele num: 118444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.245T>C
  hgvsp: ENSP00000414379.1:p.Val82Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.431T>C
  hgvsp: ENSP00000406994.1:p.Val144Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.431T>C
  hgvsp: ENSP00000414901.1:p.Val144Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.245T>C
  hgvsp: ENSP00000408472.1:p.Val82Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.494T>C
  hgvsp: ENSP00000401651.1:p.Val165Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.494T>C
  hgvsp: ENSP00000400422.1:p.Val165Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.494T>C
  hgvsp: ENSP00000377846.3:p.Val165Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.494T>C
  hgvsp: ENSP00000377845.3:p.Val165Ala
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.494T>C
  hgvsp: ENSP00000175506.4:p.Val165Ala
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val165Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-97488706-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97488706
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 97488706
    reference: chr 7
allele count: 1
allele frequency: 8.456802652053312e-6
allele num: 118248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377846
  ensembl transcript: ENST00000394309
  gene symbol: ASNS
  hgvsc: ENST00000394309.3:c.492T>G
  hgvsp: ENST00000394309.3:c.492T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000377845
  ensembl transcript: ENST00000394308
  gene symbol: ASNS
  hgvsc: ENST00000394308.3:c.492T>G
  hgvsp: ENST00000394308.3:c.492T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414901
  ensembl transcript: ENST00000422745
  gene symbol: ASNS
  hgvsc: ENST00000422745.1:c.429T>G
  hgvsp: ENST00000422745.1:c.429T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000175506
  ensembl transcript: ENST00000175506
  gene symbol: ASNS
  hgvsc: ENST00000175506.4:c.492T>G
  hgvsp: ENST00000175506.4:c.492T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000414379
  ensembl transcript: ENST00000437628
  gene symbol: ASNS
  hgvsc: ENST00000437628.1:c.243T>G
  hgvsp: ENST00000437628.1:c.243T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000408472
  ensembl transcript: ENST00000455086
  gene symbol: ASNS
  hgvsc: ENST00000455086.1:c.243T>G
  hgvsp: ENST00000455086.1:c.243T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000400422
  ensembl transcript: ENST00000442734
  gene symbol: ASNS
  hgvsc: ENST00000442734.1:c.492T>G
  hgvsp: ENST00000442734.1:c.492T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000401651
  ensembl transcript: ENST00000454046
  gene symbol: ASNS
  hgvsc: ENST00000454046.1:c.492T>G
  hgvsp: ENST00000454046.1:c.492T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000070669
  ensembl protein: ENSP00000406994
  ensembl transcript: ENST00000444334
  gene symbol: ASNS
  hgvsc: ENST00000444334.1:c.429T>G
  hgvsp: ENST00000444334.1:c.429T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/753
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5558
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu164Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-97488710-C-T
type: Variant
allele count: 1
allele frequency: 8.477162524159914e-6
allele num: 117964
alternate allele: T
canonical: true
consequence: missense
filter: PASS
hgvs: p.Gly163Asp
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 11486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2938
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523322060750084e-5
allele num: 65646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.411905e6

MQRankSum
type: SiteQuality
SIO_000300: -6.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.754e1

QD
type: SiteQuality
SIO_000300: 1.681e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.069e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

GenotypeQuality
all individuals: 9479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4156
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20668
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.418775124142823e-3
allele num: 8458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.487e0

QD
type: SiteQuality
SIO_000300: 2.967e1

VQSLOD
type: SiteQuality
SIO_000300: -1.029e0

DP
type: SiteQuality
SIO_000300: 2.480938e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

GenotypeQuality
all individuals: 1469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9308
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20663
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554243083618278e-5
allele num: 64340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13822
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

FS
type: SiteQuality
SIO_000300: 8.720000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.524e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 2.532979e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.281e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

QD
type: SiteQuality
SIO_000300: 1.12e1

GenotypeQuality
all individuals: 254
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3935
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20655
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 1.006036217303823e-4
allele num: 9940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6004
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.548e0

MQ
type: SiteQuality
SIO_000300: 6.047e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e0

QD
type: SiteQuality
SIO_000300: 1.322e1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 2.697934e6

FS
type: SiteQuality
SIO_000300: 3.196e0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 15

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 33

GenotypeQuality
all individuals: 2221
bin: 6.75e1
variant carriers: 124

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 56

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 101

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 255
bin: 3.25e1
variant carriers: 30

GenotypeQuality
all individuals: 1825
bin: 7.75e1
variant carriers: 93

GenotypeQuality
all individuals: 1026
bin: 8.75e1
variant carriers: 125

GenotypeQuality
all individuals: 43350
bin: 9.75e1
variant carriers: 31173

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 133

GenotypeQuality
all individuals: 1564
bin: 9.25e1
variant carriers: 85

East Asian
type: Population
allele count: 3642
allele frequency: 4.222119174588453e-1
allele num: 8626
num of homozygotes: 744

Latino
type: Population
allele count: 5684
allele frequency: 4.927184466019418e-1
allele num: 11536
num of homozygotes: 1445

South Asian
type: Population
allele count: 7350
allele frequency: 4.538718043719897e-1
allele num: 16194
num of homozygotes: 1658

European (Non-Finnish)
type: Population
allele count: 19346
allele frequency: 2.921562113020629e-1
allele num: 66218
num of homozygotes: 2894

European (Finnish)
type: Population
allele count: 1538
allele frequency: 2.3267776096823e-1
allele num: 6610
num of homozygotes: 185

African
type: Population
allele count: 1624
allele frequency: 1.5859375e-1
allele num: 10240
num of homozygotes: 132

Other
type: Population
allele count: 289
allele frequency: 3.232662192393736e-1
allele num: 894
num of homozygotes: 53

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

QD
type: SiteQuality
SIO_000300: 1.573e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.425894e6

MQ
type: SiteQuality
SIO_000300: 6.018e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.72e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43350
bin: 9.75e1
variant carriers: 1215

GenotypeQuality
all individuals: 1026
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 17
allele frequency: 1.66015625e-3
allele num: 10240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 407
allele frequency: 6.157337367624811e-2
allele num: 6610
num of homozygotes: 21

South Asian
type: Population
allele count: 110
allele frequency: 6.792639249104606e-3
allele num: 16194
num of homozygotes: 3

Other
type: Population
allele count: 8
allele frequency: 8.948545861297539e-3
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 678
allele frequency: 1.023890784982935e-2
allele num: 66218
num of homozygotes: 2

Latino
type: Population
allele count: 22
allele frequency: 1.907073509015257e-3
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.796429399489915e-4
allele num: 8626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

QD
type: SiteQuality
SIO_000300: 1.573e1

MQ
type: SiteQuality
SIO_000300: 6.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

DP
type: SiteQuality
SIO_000300: 3.425894e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43350
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1065
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.530490199039536e-5
allele num: 66218
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

QD
type: SiteQuality
SIO_000300: 1.573e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 3.425894e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.72e-2

MQ
type: SiteQuality
SIO_000300: 6.018e1

GenotypeQuality
all individuals: 6116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.060980398079073e-5
allele num: 66218
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

DP
type: SiteQuality
SIO_000300: 3.425894e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.72e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

QD
type: SiteQuality
SIO_000300: 1.573e1

MQ
type: SiteQuality
SIO_000300: 6.018e1

GenotypeQuality
all individuals: 3346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4455
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.522567612385805e-5
allele num: 66334
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

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

South Asian
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allele count: 2
allele frequency: 1.226542377039127e-4
allele num: 16306
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.323e1

MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

InbreedingCoeff
type: SiteQuality
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DP
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SIO_000300: 2.638755e6

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66334
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
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SIO_000300: 2.638755e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

BaseQRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: 4.58e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

FS
type: SiteQuality
SIO_000300: 4.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66482
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.6496e6

MQRankSum
type: SiteQuality
SIO_000300: -1.208e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: 4.48e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

FS
type: SiteQuality
SIO_000300: 2.814e0

GenotypeQuality
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bin: 4.75e1
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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variant carriers: 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: 11544
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.296e0

MQ
type: SiteQuality
SIO_000300: 5.75e1

DP
type: SiteQuality
SIO_000300: 2.64967e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

FS
type: SiteQuality
SIO_000300: 2.962e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
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: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.988e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.291e0

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.014e1

MQRankSum
type: SiteQuality
SIO_000300: -9.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.766999999999999e0

DP
type: SiteQuality
SIO_000300: 2.650008e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.316e0

ClippingRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Other
type: Population
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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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

Latino
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MQ
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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MQRankSum
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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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bin: 7.25e1
variant carriers: 0

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

Latino
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South Asian
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European (Non-Finnish)
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African
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East Asian
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Other
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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MQRankSum
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QD
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FS
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DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.72e-1

VQSLOD
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

QD
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SIO_000300: 1.356e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

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

Other
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allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
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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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.784735812133073e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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MQRankSum
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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SIO_000300: 8.800000000000001e-3

BaseQRankSum
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QD
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VQSLOD
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FS
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ReadPosRankSum
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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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 frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

BaseQRankSum
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SIO_000300: 3.1e0

ReadPosRankSum
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SIO_000300: 1.65e0

MQ
type: SiteQuality
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DP
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FS
type: SiteQuality
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QD
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InbreedingCoeff
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SIO_000300: 2.8e-3

ClippingRankSum
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SIO_000300: -1.091e0

VQSLOD
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SIO_000300: 6.3e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

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

African
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allele frequency: 9.902951079421667e-5
allele num: 10098
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MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.209e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 9.345000000000001e0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.037735849056604e-5
allele num: 66250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

South 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: 890
num of homozygotes: 0

African
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.19e0

MQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

QD
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SIO_000300: 1.429e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e-1

FS
type: SiteQuality
SIO_000300: 7.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.635732e6

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66228
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

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

African
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allele frequency: 9.918666931164451e-5
allele num: 10082
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11544
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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South Asian
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Other
type: Population
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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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East Asian
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Latino
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allele frequency: 3.465003465003465e-4
allele num: 11544
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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allele frequency: 2.626711061783204e-2
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Other
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.969e0

VQSLOD
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DP
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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European (Finnish)
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Other
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East Asian
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.512721991952319e-5
allele num: 66106
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
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MQRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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QD
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FS
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ClippingRankSum
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SIO_000300: -8.83e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
all individuals: 873
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 27567
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.242197253433208e-5
allele num: 16020
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.581e0

FS
type: SiteQuality
SIO_000300: 4.424e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

QD
type: SiteQuality
SIO_000300: 1.821e1

DP
type: SiteQuality
SIO_000300: 2.56793e6

VQSLOD
type: SiteQuality
SIO_000300: -8.493000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.512e0

MQ
type: SiteQuality
SIO_000300: 6.03e1

GenotypeQuality
all individuals: 773
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27847
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 914
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.612120653076284e-5
allele num: 65046
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.61e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

FS
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 2.304533e6

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

GenotypeQuality
all individuals: 3232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 131

GenotypeQuality
all individuals: 641
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

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

African
type: Population
allele count: 129
allele frequency: 1.275207591933571e-2
allele num: 10116
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 1.754693805930865e-4
allele num: 11398
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.093234056328909e-5
allele num: 12356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65046
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.61e-2

FS
type: SiteQuality
SIO_000300: 7.99e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.13e-1

DP
type: SiteQuality
SIO_000300: 2.304533e6

GenotypeQuality
all individuals: 275
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3444
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variant carriers: 0

GenotypeQuality
all individuals: 27794
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65052
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.305753e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

FS
type: SiteQuality
SIO_000300: 3.003e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 819
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
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variant carriers: 0

GenotypeQuality
all individuals: 3620
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variant carriers: 0

GenotypeQuality
all individuals: 27920
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variant carriers: 1

GenotypeQuality
all individuals: 684
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variant carriers: 0

GenotypeQuality
all individuals: 2334
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variant carriers: 0

GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 153
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GenotypeQuality
all individuals: 3659
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5952
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variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.838646202282565e-5
allele num: 10164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.22e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.752e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.315107e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3659
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3680
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variant carriers: 0

GenotypeQuality
all individuals: 794
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 336
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2358
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variant carriers: 0

GenotypeQuality
all individuals: 27947
bin: 9.75e1
variant carriers: 6

African
type: Population
allele count: 1
allele frequency: 9.8405825624877e-5
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.660487206986364e-5
allele num: 65270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

DP
type: SiteQuality
SIO_000300: 2.324665e6

FS
type: SiteQuality
SIO_000300: 1.985e0

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 2424
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3860
bin: 6.75e1
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: 65398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12896
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.586e0

FS
type: SiteQuality
SIO_000300: 4.956e0

VQSLOD
type: SiteQuality
SIO_000300: -2.805e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: -1.928e0

DP
type: SiteQuality
SIO_000300: 2.341042e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.165e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.13e1

GenotypeQuality
all individuals: 28037
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3738
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variant carriers: 0

GenotypeQuality
all individuals: 2420
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12918
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.777082518576456e-5
allele num: 10228
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: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65432
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 2.342855e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.161e1

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3771
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
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GenotypeQuality
all individuals: 2450
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28068
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 1.75e1
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: 1
allele frequency: 1.52597204419215e-5
allele num: 65532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.767e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.061e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

FS
type: SiteQuality
SIO_000300: 1.149e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 2.35057e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 3796
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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
all individuals: 8070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
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: 65658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.388567461235825e-3
allele num: 8642
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 2.211e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.358487e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 2470
bin: 8.75e1
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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 289
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52151421094273e-5
allele num: 65724
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: 10354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.362289e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.332e0

QD
type: SiteQuality
SIO_000300: 1.021e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.019961948479449e-5
allele num: 66226
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: 15062
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: -4.993e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

DP
type: SiteQuality
SIO_000300: 2.387419e6

FS
type: SiteQuality
SIO_000300: 7.694e0

QD
type: SiteQuality
SIO_000300: 1.504e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

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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bin: 7.25e1
variant carriers: 0

Latino
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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: 888
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15180
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66276
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1865e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 2.389693e6

QD
type: SiteQuality
SIO_000300: 2.133e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 6.068e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.977e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2517
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511142522029412e-5
allele num: 66502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.043e0

QD
type: SiteQuality
SIO_000300: 1.06e1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

FS
type: SiteQuality
SIO_000300: 1.481e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.94e-1

DP
type: SiteQuality
SIO_000300: 2.402787e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 43
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variant carriers: 0

GenotypeQuality
all individuals: 4423
bin: 6.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.22975330176925e-5
allele num: 16052
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

DP
type: SiteQuality
SIO_000300: 2.408654e6

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

FS
type: SiteQuality
SIO_000300: 4.078e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

QD
type: SiteQuality
SIO_000300: 1.127e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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
all individuals: 33
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

Latino
type: Population
allele count: 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: 16254
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: 2.415619e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

QD
type: SiteQuality
SIO_000300: 1.86e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.73e-1

FS
type: SiteQuality
SIO_000300: 5.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.486e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 64

GenotypeQuality
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variant carriers: 56991

GenotypeQuality
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GenotypeQuality
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variant carriers: 18

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 42

GenotypeQuality
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variant carriers: 144

GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 95

GenotypeQuality
all individuals: 1751
bin: 6.25e1
variant carriers: 56

East Asian
type: Population
allele count: 7803
allele frequency: 9.016639704183037e-1
allele num: 8654
num of homozygotes: 3515

African
type: Population
allele count: 9866
allele frequency: 9.481068614261003e-1
allele num: 10406
num of homozygotes: 4683

Other
type: Population
allele count: 720
allele frequency: 7.929515418502202e-1
allele num: 908
num of homozygotes: 282

Latino
type: Population
allele count: 9543
allele frequency: 8.242356192779409e-1
allele num: 11578
num of homozygotes: 3942

South Asian
type: Population
allele count: 13813
allele frequency: 8.371515151515152e-1
allele num: 16500
num of homozygotes: 5815

European (Non-Finnish)
type: Population
allele count: 49617
allele frequency: 7.43660071942446e-1
allele num: 66720
num of homozygotes: 18506

European (Finnish)
type: Population
allele count: 5108
allele frequency: 7.723011793166011e-1
allele num: 6614
num of homozygotes: 1980

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.86e-2

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

DP
type: SiteQuality
SIO_000300: 5.91876e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.23e0

QD
type: SiteQuality
SIO_000300: 2.642e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1732
bin: 8.75e1
variant carriers: 0

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 5.362e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.05e0

ReadPosRankSum
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SIO_000300: 4.91e-1

MQRankSum
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SIO_000300: -6.66e-1

QD
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ClippingRankSum
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SIO_000300: -1.145e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.433291e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.12e-2

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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FS
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MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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SIO_000300: -7.05e-1

ClippingRankSum
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SIO_000300: -3.3e-1

MQRankSum
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ReadPosRankSum
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SIO_000300: 8.02e-1

QD
type: SiteQuality
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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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variant carriers: 0

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

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

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

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

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

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

South Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -9.46e-1

ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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FS
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SIO_000300: 8.561999999999999e0

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.0428e1

QD
type: SiteQuality
SIO_000300: 2.769e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
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MQ
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SIO_000300: 5.971e1

MQRankSum
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SIO_000300: 1.6e-1

BaseQRankSum
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SIO_000300: 6.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.432566e6

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.922e1

QD
type: SiteQuality
SIO_000300: 1.436e1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
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 frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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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
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 2.59e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 66
allele frequency: 7.626531083891842e-3
allele num: 8654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

DP
type: SiteQuality
SIO_000300: 2.433276e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-2

QD
type: SiteQuality
SIO_000300: 1.256e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.275e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.57e-1

FS
type: SiteQuality
SIO_000300: 2.234e0

DP
type: SiteQuality
SIO_000300: 2.426152e6

GenotypeQuality
all individuals: 19561
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8654
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.077e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.55e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.425915e6

MQRankSum
type: SiteQuality
SIO_000300: -1.761e0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20103
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

FS
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 2.423394e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.04e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.35e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 3775
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GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.47e-1

DP
type: SiteQuality
SIO_000300: 2.42116e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 6.354e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

QD
type: SiteQuality
SIO_000300: 1.078e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.84e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 30
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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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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.411e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

FS
type: SiteQuality
SIO_000300: 4.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.291e0

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

GenotypeQuality
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bin: 3.25e1
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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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: 10222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

European (Finnish)
type: Population
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: 11568
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.786e0

DP
type: SiteQuality
SIO_000300: 2.41316e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
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: 11564
num of homozygotes: 0

South 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: 10200
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504257047444267e-5
allele num: 66478
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.885843600704048e-4
allele num: 15908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.546e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.033e0

QD
type: SiteQuality
SIO_000300: 1.268e1

FS
type: SiteQuality
SIO_000300: 8.861000000000001e0

DP
type: SiteQuality
SIO_000300: 2.397177e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
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: 11542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.279099513942185e-4
allele num: 15636
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: 2.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 2.380364e6

QD
type: SiteQuality
SIO_000300: 1.235e1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15624
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020053152935492e-5
allele num: 66224
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.887284951552304e-5
allele num: 10114
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

QD
type: SiteQuality
SIO_000300: 1.337e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.133e0

FS
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 2.378718e6

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
all individuals: 20075
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variant carriers: 5

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510619656182966e-5
allele num: 66198
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15544
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.972651605231867e-4
allele num: 10092
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

DP
type: SiteQuality
SIO_000300: 2.374532e6

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

FS
type: SiteQuality
SIO_000300: 2.115e0

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.375e1

GenotypeQuality
all individuals: 3699
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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
all individuals: 5940
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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: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.432522835456066e-5
allele num: 15546
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.900990099009902e-5
allele num: 10100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021239312365933e-5
allele num: 66198
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: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.37367e6

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

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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bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66128
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.496037417175523e-5
allele num: 15394
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

DP
type: SiteQuality
SIO_000300: 2.364492e6

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

QD
type: SiteQuality
SIO_000300: 1.56e1

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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bin: 6.25e1
variant carriers: 1

South Asian
type: Population
allele count: 15
allele frequency: 9.744056125763284e-4
allele num: 15394
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.364492e6

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

QD
type: SiteQuality
SIO_000300: 1.56e1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.729e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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VQSLOD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.135e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15086
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65992
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.349482e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 1.434e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

QD
type: SiteQuality
SIO_000300: 1.234e1

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

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15751
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20054
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3118
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14934
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.736714136853074e-4
allele num: 11516
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

QD
type: SiteQuality
SIO_000300: 1.55e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

DP
type: SiteQuality
SIO_000300: 2.34111e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1706
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20052
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.002807862013638e-4
allele num: 9972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.335063e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: -1.021e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

QD
type: SiteQuality
SIO_000300: 2.277e1