6-109980407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980407
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980407
    reference: chr 6
allele count: 1
allele frequency: 9.029834573430615e-6
allele num: 110744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.98+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2134+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.630+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.399+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.630+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.630+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.293+24C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.630+24C>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16887
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6219
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

6-109980413-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980413
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980413
    reference: chr 6
allele count: 4
allele frequency: 3.576026319553712e-5
allele num: 111856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.399+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.630+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.293+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.630+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2134+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.98+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.630+18A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.630+18A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16990
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27270
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

6-109980413-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980413
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980412
    reference: chr 6
allele count: 4
allele frequency: 3.576026319553712e-5
allele num: 111856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.293+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.630+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.630+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2134+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.630+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.98+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.399+17delT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.630+17delT
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16990
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6782
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: TA
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

6-109980427-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980427
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980427
    reference: chr 6
allele count: 4
allele frequency: 3.496197884800279e-5
allele num: 114410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.630+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.98+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.293+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.630+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.399+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.630+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2134+4A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.630+4A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17242
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2046
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
hgvs: c.630+4A>G
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

6-109980431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980431
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980431
    reference: chr 6
allele count: 2
allele frequency: 1.758705592683785e-5
allele num: 113720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.399G>A
  hgvsp: ENST00000448084.2:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.630G>A
  hgvsp: ENST00000285397.5:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2134G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.98G>A
  hgvsp: ENST00000605986.1:c.98G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.293G>A
  hgvsp: ENST00000524674.1:c.293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.630G>A
  hgvsp: ENST00000532976.1:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.630G>A
  hgvsp: ENST00000424296.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.630G>A
  hgvsp: ENST00000368948.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6498
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
hgvs: c.630G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

6-109980431-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980431
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980428
    reference: chr 6
allele count: 22
allele frequency: 1.934576151952163e-4
allele num: 113720
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.627_629delAGA
  hgvsp: ENSP00000410186.2:p.Glu210del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.627_629delAGA
  hgvsp: ENSP00000436325.1:p.Glu210del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.290_292delAGA
  hgvsp: ENSP00000431394.1:p.Glu98del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.95_97delAGA
  hgvsp: ENSP00000475585.1:p.Glu33del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.396_398delAGA
  hgvsp: ENSP00000407510.2:p.Glu133del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.627_629delAGA
  hgvsp: ENSP00000285397.4:p.Glu210del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.627_629delAGA
  hgvsp: ENSP00000357944.2:p.Glu210del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2137_-2135delAGA
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17918
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 3
hgvs: p.Glu210del
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: CTCT
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

6-109980445-GCTCTTCTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980445
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980436
    reference: chr 6
allele count: 25
allele frequency: 2.133615539548698e-4
allele num: 117172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.376_384delGAAGAAGAG
  hgvsp: ENSP00000407510.2:p.Glu126_Glu128del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.607_615delGAAGAAGAG
  hgvsp: ENSP00000410186.2:p.Glu203_Glu205del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.75_83delGAAGAAGAG
  hgvsp: ENSP00000475585.1:p.Glu26_Glu28del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.607_615delGAAGAAGAG
  hgvsp: ENSP00000357944.2:p.Glu203_Glu205del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.607_615delGAAGAAGAG
  hgvsp: ENSP00000285397.4:p.Glu203_Glu205del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.607_615delGAAGAAGAG
  hgvsp: ENSP00000436325.1:p.Glu203_Glu205del
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.270_278delGAAGAAGAG
  hgvsp: ENSP00000431394.1:p.Glu91_Glu93del
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9663
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16733
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 9.75e1
  variant carriers: 25
hgvs: p.Glu203_Glu205del
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: GCTCTTCTTC
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-109980452-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980452
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980452
    reference: chr 6
allele count: 1
allele frequency: 8.451799388089724e-6
allele num: 118318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.77A>T
  hgvsp: ENSP00000475585.1:p.Glu26Asp
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.609A>T
  hgvsp: ENSP00000357944.2:p.Glu203Asp
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2155A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.609A>T
  hgvsp: ENSP00000436325.1:p.Glu203Asp
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.609A>T
  hgvsp: ENSP00000410186.2:p.Glu203Asp
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.609A>T
  hgvsp: ENSP00000285397.4:p.Glu203Asp
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.272A>T
  hgvsp: ENSP00000431394.1:p.Glu91Asp
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.378A>T
  hgvsp: ENSP00000407510.2:p.Glu126Asp
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu203Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

6-109980464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980464
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980464
    reference: chr 6
allele count: 1
allele frequency: 8.383775717232013e-6
allele num: 119278
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.597G>A
  hgvsp: ENST00000424296.2:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.260G>A
  hgvsp: ENST00000524674.1:c.260G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.597G>A
  hgvsp: ENST00000285397.5:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.597G>A
  hgvsp: ENST00000368948.2:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.65G>A
  hgvsp: ENST00000605986.1:c.65G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2167G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.597G>A
  hgvsp: ENST00000532976.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.366G>A
  hgvsp: ENST00000448084.2:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17353
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu199Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-109980478-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980478
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980478
    reference: chr 6
allele count: 1
allele frequency: 8.344180768332166e-6
allele num: 119844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2181G>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.583G>T
  hgvsp: ENSP00000357944.2:p.Gly195Ter
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.246G>T
  hgvsp: ENSP00000431394.1:p.Gly83Ter
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.583G>T
  hgvsp: ENSP00000410186.2:p.Gly195Ter
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.583G>T
  hgvsp: ENSP00000285397.4:p.Gly195Ter
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.583G>T
  hgvsp: ENSP00000436325.1:p.Gly195Ter
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.51G>T
  hgvsp: ENSP00000475585.1:p.Gly18Ter
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.352G>T
  hgvsp: ENSP00000407510.2:p.Gly118Ter
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly195Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

6-109980478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980478
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980478
    reference: chr 6
allele count: 2
allele frequency: 1.668836153666433e-5
allele num: 119844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.583G>A
  hgvsp: ENSP00000285397.4:p.Gly195Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2181G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.246G>A
  hgvsp: ENSP00000431394.1:p.Gly83Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.352G>A
  hgvsp: ENSP00000407510.2:p.Gly118Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.583G>A
  hgvsp: ENSP00000357944.2:p.Gly195Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.583G>A
  hgvsp: ENSP00000436325.1:p.Gly195Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.51G>A
  hgvsp: ENSP00000475585.1:p.Gly18Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.583G>A
  hgvsp: ENSP00000410186.2:p.Gly195Arg
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6771
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly195Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

6-109980479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980479
    reference: chr 6
allele count: 29
allele frequency: 2.417593410807476e-4
allele num: 119954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2182C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.245C>T
  hgvsp: ENST00000524674.1:c.245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.582C>T
  hgvsp: ENST00000285397.5:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.582C>T
  hgvsp: ENST00000368948.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.582C>T
  hgvsp: ENST00000532976.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.50C>T
  hgvsp: ENST00000605986.1:c.50C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.351C>T
  hgvsp: ENST00000448084.2:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.582C>T
  hgvsp: ENST00000424296.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17936
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23349
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3901
  bin: 9.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp194Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-109980487-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980487
    reference: chr 6
allele count: 20
allele frequency: 1.664918502239315e-4
allele num: 120126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.42C>G
  hgvsp: ENSP00000475585.1:p.Gln15Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.574C>G
  hgvsp: ENSP00000357944.2:p.Gln192Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.574C>G
  hgvsp: ENSP00000410186.2:p.Gln192Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.237C>G
  hgvsp: ENSP00000431394.1:p.Gln80Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.343C>G
  hgvsp: ENSP00000407510.2:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.574C>G
  hgvsp: ENSP00000436325.1:p.Gln192Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.574C>G
  hgvsp: ENSP00000285397.4:p.Gln192Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2190C>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10039
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23735
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18252
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6906
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln192Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

6-109980489-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980489
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980489
    reference: chr 6
allele count: 4
allele frequency: 3.326901324106727e-5
allele num: 120232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.572C>G
  hgvsp: ENSP00000357944.2:p.Ala191Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.572C>G
  hgvsp: ENSP00000410186.2:p.Ala191Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.235C>G
  hgvsp: ENSP00000431394.1:p.Ala79Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.572C>G
  hgvsp: ENSP00000436325.1:p.Ala191Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.40C>G
  hgvsp: ENSP00000475585.1:p.Ala14Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.341C>G
  hgvsp: ENSP00000407510.2:p.Ala114Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.572C>G
  hgvsp: ENSP00000285397.4:p.Ala191Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2192C>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala191Gly
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

6-109980495-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980495
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980495
    reference: chr 6
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2198A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.566A>G
  hgvsp: ENSP00000357944.2:p.Lys189Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.34A>G
  hgvsp: ENSP00000475585.1:p.Lys12Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.566A>G
  hgvsp: ENSP00000436325.1:p.Lys189Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.229A>G
  hgvsp: ENSP00000431394.1:p.Lys77Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.566A>G
  hgvsp: ENSP00000410186.2:p.Lys189Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.566A>G
  hgvsp: ENSP00000285397.4:p.Lys189Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.335A>G
  hgvsp: ENSP00000407510.2:p.Lys112Arg
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42113
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys189Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

6-109980496-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980496
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980496
    reference: chr 6
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.228A>G
  hgvsp: ENSP00000431394.1:p.Lys77Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2199A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.565A>G
  hgvsp: ENSP00000285397.4:p.Lys189Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.565A>G
  hgvsp: ENSP00000410186.2:p.Lys189Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.565A>G
  hgvsp: ENSP00000436325.1:p.Lys189Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.33A>G
  hgvsp: ENSP00000475585.1:p.Lys12Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.334A>G
  hgvsp: ENSP00000407510.2:p.Lys112Glu
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.565A>G
  hgvsp: ENSP00000357944.2:p.Lys189Glu
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7030
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys189Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/6-109980500-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980500
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980500
    reference: chr 6
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.561G>T
  hgvsp: ENSP00000285397.4:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.29G>T
  hgvsp: ENSP00000475585.1:p.Lys10Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.224G>T
  hgvsp: ENSP00000431394.1:p.Lys75Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2203G>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.561G>T
  hgvsp: ENSP00000410186.2:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.561G>T
  hgvsp: ENSP00000436325.1:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.561G>T
  hgvsp: ENSP00000357944.2:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.330G>T
  hgvsp: ENSP00000407510.2:p.Lys110Asn
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys187Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

6-109980500-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980500
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980500
    reference: chr 6
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.29G>C
  hgvsp: ENSP00000475585.1:p.Lys10Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.561G>C
  hgvsp: ENSP00000357944.2:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.561G>C
  hgvsp: ENSP00000285397.4:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.561G>C
  hgvsp: ENSP00000436325.1:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.561G>C
  hgvsp: ENSP00000410186.2:p.Lys187Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2203G>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.330G>C
  hgvsp: ENSP00000407510.2:p.Lys110Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.224G>C
  hgvsp: ENSP00000431394.1:p.Lys75Asn
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys187Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

6-109980510-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980510
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980510
    reference: chr 6
allele count: 2
allele frequency: 1.65218253312626e-5
allele num: 121052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.551A>G
  hgvsp: ENSP00000436325.1:p.His184Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.19A>G
  hgvsp: ENSP00000475585.1:p.His7Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.551A>G
  hgvsp: ENSP00000410186.2:p.His184Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.551A>G
  hgvsp: ENSP00000285397.4:p.His184Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.214A>G
  hgvsp: ENSP00000431394.1:p.His72Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2213A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.551A>G
  hgvsp: ENSP00000357944.2:p.His184Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.320A>G
  hgvsp: ENSP00000407510.2:p.His107Arg
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His184Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

6-109980513-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980513
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980513
    reference: chr 6
allele count: 2
allele frequency: 1.65180046250413e-5
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.548A>G
  hgvsp: ENSP00000357944.2:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.548A>G
  hgvsp: ENSP00000436325.1:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.317A>G
  hgvsp: ENSP00000407510.2:p.Asn106Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2216A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.16A>G
  hgvsp: ENSP00000475585.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.548A>G
  hgvsp: ENSP00000285397.4:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.211A>G
  hgvsp: ENSP00000431394.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.548A>G
  hgvsp: ENSP00000410186.2:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42746
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn183Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-109980517-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980517
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980517
    reference: chr 6
allele count: 2
allele frequency: 1.651473114017704e-5
allele num: 121104
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.544G>C
  hgvsp: ENSP00000410186.2:p.Glu182Gln
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.207G>C
  hgvsp: ENSP00000431394.1:p.Glu70Gln
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.544G>C
  hgvsp: ENSP00000436325.1:p.Glu182Gln
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.544G>C
  hgvsp: ENSP00000357944.2:p.Glu182Gln
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.12G>C
  hgvsp: ENSP00000475585.1:p.Glu5Gln
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.313G>C
  hgvsp: ENSP00000407510.2:p.Glu105Gln
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2220G>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.544G>C
  hgvsp: ENSP00000285397.4:p.Glu182Gln
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu182Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-109980519-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980519
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980519
    reference: chr 6
allele count: 6
allele frequency: 4.954010271314629e-5
allele num: 121114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000475585
  ensembl transcript: ENST00000605986
  gene symbol: AK9
  hgvsc: ENST00000605986.1:c.10T>C
  hgvsp: ENSP00000475585.1:p.Ile4Thr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.542T>C
  hgvsp: ENSP00000357944.2:p.Ile181Thr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.542T>C
  hgvsp: ENSP00000410186.2:p.Ile181Thr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.542T>C
  hgvsp: ENSP00000436325.1:p.Ile181Thr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.542T>C
  hgvsp: ENSP00000285397.4:p.Ile181Thr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.311T>C
  hgvsp: ENSP00000407510.2:p.Ile104Thr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2222T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.205T>C
  hgvsp: ENSP00000431394.1:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7075
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile181Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/6-109980532-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980532
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980532
    reference: chr 6
allele count: 52
allele frequency: 4.291420460172317e-4
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.529G>T
  hgvsp: ENSP00000357944.2:p.Asp177Tyr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.192G>T
  hgvsp: ENSP00000431394.1:p.Asp65Tyr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.529G>T
  hgvsp: ENSP00000410186.2:p.Asp177Tyr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.529G>T
  hgvsp: ENSP00000285397.4:p.Asp177Tyr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.529G>T
  hgvsp: ENSP00000436325.1:p.Asp177Tyr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.298G>T
  hgvsp: ENSP00000407510.2:p.Asp100Tyr
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2235G>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp177Tyr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-109980544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980544
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980544
    reference: chr 6
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.517A>G
  hgvsp: ENSP00000436325.1:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.517A>G
  hgvsp: ENSP00000285397.4:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.517A>G
  hgvsp: ENSP00000410186.2:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2247A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.517A>G
  hgvsp: ENSP00000357944.2:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.286A>G
  hgvsp: ENSP00000407510.2:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.180A>G
  hgvsp: ENSP00000431394.1:p.Arg61Gly
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg173Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

6-109980546-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980546
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980546
    reference: chr 6
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.515G>A
  hgvsp: ENSP00000357944.2:p.Ser172Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.284G>A
  hgvsp: ENSP00000407510.2:p.Ser95Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.515G>A
  hgvsp: ENSP00000410186.2:p.Ser172Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.515G>A
  hgvsp: ENSP00000285397.4:p.Ser172Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.515G>A
  hgvsp: ENSP00000436325.1:p.Ser172Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.178G>A
  hgvsp: ENSP00000431394.1:p.Ser60Asn
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2249G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7087
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser172Asn
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-109980549-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980549
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980549
    reference: chr 6
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.281A>G
  hgvsp: ENSP00000407510.2:p.Tyr94Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.512A>G
  hgvsp: ENSP00000285397.4:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.512A>G
  hgvsp: ENSP00000436325.1:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.512A>G
  hgvsp: ENSP00000357944.2:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2252A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.175A>G
  hgvsp: ENSP00000431394.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.512A>G
  hgvsp: ENSP00000410186.2:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr171Cys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

6-109980551-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980551
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980551
    reference: chr 6
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.173A>G
  hgvsp: ENSP00000431394.1:p.Ile58Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.279A>G
  hgvsp: ENSP00000407510.2:p.Ile93Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.510A>G
  hgvsp: ENSP00000285397.4:p.Ile170Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.510A>G
  hgvsp: ENSP00000436325.1:p.Ile170Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.510A>G
  hgvsp: ENSP00000357944.2:p.Ile170Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.510A>G
  hgvsp: ENSP00000410186.2:p.Ile170Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2254A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile170Met
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

6-109980553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980553
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980553
    reference: chr 6
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.277A>G
  hgvsp: ENSP00000407510.2:p.Ile93Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.508A>G
  hgvsp: ENSP00000410186.2:p.Ile170Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.508A>G
  hgvsp: ENSP00000436325.1:p.Ile170Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.508A>G
  hgvsp: ENSP00000285397.4:p.Ile170Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.171A>G
  hgvsp: ENSP00000431394.1:p.Ile58Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.508A>G
  hgvsp: ENSP00000357944.2:p.Ile170Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2256A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile170Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-109980554-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980554
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980554
    reference: chr 6
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.507C>T
  hgvsp: ENST00000285397.5:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.170C>T
  hgvsp: ENST00000524674.1:c.170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.507C>T
  hgvsp: ENST00000424296.2:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.276C>T
  hgvsp: ENST00000448084.2:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.507C>T
  hgvsp: ENST00000368948.2:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2257C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.507C>T
  hgvsp: ENST00000532976.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1879
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr169Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-109980555-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980555
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980555
    reference: chr 6
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.506A>G
  hgvsp: ENSP00000410186.2:p.Tyr169Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.169A>G
  hgvsp: ENSP00000431394.1:p.Tyr57Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2258A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.506A>G
  hgvsp: ENSP00000357944.2:p.Tyr169Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.506A>G
  hgvsp: ENSP00000436325.1:p.Tyr169Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.275A>G
  hgvsp: ENSP00000407510.2:p.Tyr92Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.506A>G
  hgvsp: ENSP00000285397.4:p.Tyr169Cys
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr169Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-109980557-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980557
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980557
    reference: chr 6
allele count: 2
allele frequency: 1.650083329208125e-5
allele num: 121206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.504A>C
  hgvsp: ENST00000285397.5:c.504A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.167A>C
  hgvsp: ENST00000524674.1:c.167A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.504A>C
  hgvsp: ENST00000532976.1:c.504A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.504A>C
  hgvsp: ENST00000368948.2:c.504A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.273A>C
  hgvsp: ENST00000448084.2:c.273A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.504A>C
  hgvsp: ENST00000424296.2:c.504A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2260A>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3836
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly168Gly
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

6-109980560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980560
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980560
    reference: chr 6
allele count: 10
allele frequency: 8.250552787036731e-5
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.164G>A
  hgvsp: ENST00000524674.1:c.164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.501G>A
  hgvsp: ENST00000368948.2:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2263G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.270G>A
  hgvsp: ENST00000448084.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.501G>A
  hgvsp: ENST00000532976.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.501G>A
  hgvsp: ENST00000285397.5:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.501G>A
  hgvsp: ENST00000424296.2:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr167Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

6-109980561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980561
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980561
    reference: chr 6
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2264C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.500C>T
  hgvsp: ENSP00000436325.1:p.Thr167Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.500C>T
  hgvsp: ENSP00000410186.2:p.Thr167Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.269C>T
  hgvsp: ENSP00000407510.2:p.Thr90Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.500C>T
  hgvsp: ENSP00000285397.4:p.Thr167Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.163C>T
  hgvsp: ENSP00000431394.1:p.Thr55Met
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.500C>T
  hgvsp: ENSP00000357944.2:p.Thr167Met
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr167Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

6-109980579-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980579
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980579
    reference: chr 6
allele count: 2
allele frequency: 1.650301179965344e-5
allele num: 121190
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.482A>G
  hgvsp: ENSP00000410186.2:p.Gln161Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.482A>G
  hgvsp: ENSP00000436325.1:p.Gln161Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.251A>G
  hgvsp: ENSP00000407510.2:p.Gln84Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.145A>G
  hgvsp: ENSP00000431394.1:p.Gln49Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2282A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.482A>G
  hgvsp: ENSP00000285397.4:p.Gln161Arg
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.482A>G
  hgvsp: ENSP00000357944.2:p.Gln161Arg
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln161Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/6-109980582-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980582
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980582
    reference: chr 6
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.479G>T
  hgvsp: ENSP00000410186.2:p.Gly160Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2285G>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.479G>T
  hgvsp: ENSP00000285397.4:p.Gly160Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.479G>T
  hgvsp: ENSP00000357944.2:p.Gly160Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.142G>T
  hgvsp: ENSP00000431394.1:p.Gly48Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.479G>T
  hgvsp: ENSP00000436325.1:p.Gly160Val
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.248G>T
  hgvsp: ENSP00000407510.2:p.Gly83Val
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly160Val
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-109980586-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980586
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980586
    reference: chr 6
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.475T>G
  hgvsp: ENSP00000357944.2:p.Ser159Ala
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.475T>G
  hgvsp: ENSP00000436325.1:p.Ser159Ala
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.475T>G
  hgvsp: ENSP00000410186.2:p.Ser159Ala
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.244T>G
  hgvsp: ENSP00000407510.2:p.Ser82Ala
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.475T>G
  hgvsp: ENSP00000285397.4:p.Ser159Ala
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2289T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.138T>G
  hgvsp: ENSP00000431394.1:p.Ser47Ala
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7080
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3834
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser159Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS

6-109980599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980599
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980599
    reference: chr 6
allele count: 3
allele frequency: 2.477250582153887e-5
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.462G>A
  hgvsp: ENST00000368948.2:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.462G>A
  hgvsp: ENST00000285397.5:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.462G>A
  hgvsp: ENST00000424296.2:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.231G>A
  hgvsp: ENST00000448084.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.125G>A
  hgvsp: ENST00000524674.1:c.125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2302G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.462G>A
  hgvsp: ENST00000532976.1:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu154Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

6-109980606-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980606
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980606
    reference: chr 6
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.118A>G
  hgvsp: ENSP00000431394.1:p.Tyr40Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.224A>G
  hgvsp: ENSP00000407510.2:p.Tyr75Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.455A>G
  hgvsp: ENSP00000436325.1:p.Tyr152Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.455A>G
  hgvsp: ENSP00000285397.4:p.Tyr152Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2309A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.455A>G
  hgvsp: ENSP00000410186.2:p.Tyr152Cys
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.455A>G
  hgvsp: ENSP00000357944.2:p.Tyr152Cys
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr152Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

6-109980608-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980608
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980608
    reference: chr 6
allele count: 2
allele frequency: 1.652592090694254e-5
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.453C>T
  hgvsp: ENST00000368948.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.453C>T
  hgvsp: ENST00000285397.5:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2311C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.453C>T
  hgvsp: ENST00000424296.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.453C>T
  hgvsp: ENST00000532976.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.116C>T
  hgvsp: ENST00000524674.1:c.116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.222C>T
  hgvsp: ENST00000448084.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp151Asp
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-109980613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980613
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980613
    reference: chr 6
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.217C>T
  hgvsp: ENSP00000407510.2:p.Pro73Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.448C>T
  hgvsp: ENSP00000285397.4:p.Pro150Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.448C>T
  hgvsp: ENSP00000357944.2:p.Pro150Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.448C>T
  hgvsp: ENSP00000410186.2:p.Pro150Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2316C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.111C>T
  hgvsp: ENSP00000431394.1:p.Pro38Ser
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.448C>T
  hgvsp: ENSP00000436325.1:p.Pro150Ser
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3833
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro150Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-109980618-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980618
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980618
    reference: chr 6
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-2A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-2A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-2A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-2A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-2A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-2A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-2A>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1870
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 8.25e1
  variant carriers: 0
hgvs: c.445-2A>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-109980621-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980621
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980621
    reference: chr 6
allele count: 3
allele frequency: 2.485871961021528e-5
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-5C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-5C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-5C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-5C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-5C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-5C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-5C>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24286
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42192
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 2.25e1
  variant carriers: 0
hgvs: c.445-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

6-109980622-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980622
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980622
    reference: chr 6
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-6T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-6T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-6T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-6T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-6T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-6T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-6T>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41997
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3834
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
hgvs: c.445-6T>C
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-109980622-AAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980622
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980619
    reference: chr 6
allele count: 2
allele frequency: 1.658457303016734e-5
allele num: 120594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-9_445-7delGTT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-9_445-7delGTT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-9_-2319-7delGTT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-9_108-7delGTT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-9_445-7delGTT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-9_214-7delGTT
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-9_445-7delGTT
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6980
  bin: 6.75e1
  variant carriers: 0
hgvs: c.445-9_445-7delGTT
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: AAAC
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

6-109980628-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980628
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980628
    reference: chr 6
allele count: 91
allele frequency: 7.564548039036393e-4
allele num: 120298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-12G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-12G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-12G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-12G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-12G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-12G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-12G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23966
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17832
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 6887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

6-109980632-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980632
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980632
    reference: chr 6
allele count: 44
allele frequency: 3.666238938790474e-4
allele num: 120014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-16T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-16T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-16T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-16T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-16T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-16T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-16T>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17374
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23578
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40456
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6877
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-109980643-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980643
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980643
    reference: chr 6
allele count: 2
allele frequency: 1.680983038881138e-5
allele num: 118978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-27A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-27A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-27A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-27A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-27A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-27A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-27A>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6077
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

6-109980652-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980652
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980652
    reference: chr 6
allele count: 1
allele frequency: 8.450513791238508e-6
allele num: 118336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-36A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-36A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-36A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-36A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-36A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-36A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-36A>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4243
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

6-109980660-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980660
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980660
    reference: chr 6
allele count: 1
allele frequency: 8.519919571959241e-6
allele num: 117372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-44C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-44C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-44C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-44C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-44C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-44C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-44C>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4608
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4449
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

6-109980661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109980661
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109980661
    reference: chr 6
allele count: 1
allele frequency: 8.557833841098141e-6
allele num: 116852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-45G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-45G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-45G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-45G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-45G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-45G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-45G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11510
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5075
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4422
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

6-109982114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982114
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982114
    reference: chr 6
allele count: 11
allele frequency: 9.934791640324416e-5
allele num: 110722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1498A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1498A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1498A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1498A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1498A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1498A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1498A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19288
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-109982114-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982114
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982114
    reference: chr 6
allele count: 1
allele frequency: 9.031628763931287e-6
allele num: 110722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1498A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1498A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1498A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1498A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1498A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1498A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1498A>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8039
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-109982115-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982115
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982115
    reference: chr 6
allele count: 1
allele frequency: 9.030486923854934e-6
allele num: 110736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1499A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1499A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1499A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1499A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1499A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1499A>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1499A>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

6-109982120-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982120
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982120
    reference: chr 6
allele count: 1
allele frequency: 9.027389098524925e-6
allele num: 110774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1504C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1504C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1504C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1504C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1504C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1504C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1504C>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3673
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

6-109982132-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982132
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982132
    reference: chr 6
allele count: 1
allele frequency: 9.02380479705463e-6
allele num: 110818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1516C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1516C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1516C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1516C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1516C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1516C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1516C>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2700
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19291
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3718
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4932
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

6-109982139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982139
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982139
    reference: chr 6
allele count: 1
allele frequency: 9.004466215242761e-6
allele num: 111056
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1523C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1523C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1523C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1523C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1523C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1523C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1523C>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3775
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3995
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

6-109982142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982142
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982142
    reference: chr 6
allele count: 74
allele frequency: 6.662465112091474e-4
allele num: 111070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1526C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1526C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1526C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1526C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1526C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1526C>T
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1526C>T
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9437
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10287
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5073
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3780
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

6-109982143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982143
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982143
    reference: chr 6
allele count: 1
allele frequency: 9.00284489898808e-6
allele num: 111076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1527G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1527G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1527G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1527G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1527G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1527G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1527G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3798
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5086
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

6-109982145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982145
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982145
    reference: chr 6
allele count: 13
allele frequency: 1.169990640074879e-4
allele num: 111112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1529G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1529G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1529G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1529G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1529G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1529G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1529G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4012
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11861
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-109982147-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982147
    reference: chr 6
allele count: 1
allele frequency: 9.000414019044876e-6
allele num: 111106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1531C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1531C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1531C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1531C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1531C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1531C>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1531C>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5058
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

6-109982147-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982147
    reference: chr 6
allele count: 1
allele frequency: 9.000414019044876e-6
allele num: 111106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1531C>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1531C>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1531C>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1531C>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1531C>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1531C>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1531C>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11219
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19315
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4024
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-109982150-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982150
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982150
    reference: chr 6
allele count: 1
allele frequency: 8.995070701255712e-6
allele num: 111172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1534A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1534A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1534A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1534A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1534A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1534A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1534A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3830
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4047
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS

6-109982160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982160
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982160
    reference: chr 6
allele count: 75873
allele frequency: 6.785644015955068e-1
allele num: 111814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1544G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1544G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1544G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1544G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1544G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1544G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1544G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 3.25e1
  variant carriers: 6208
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 6.75e1
  variant carriers: 1331
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 5.25e1
  variant carriers: 4345
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 856
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 657
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 6.25e1
  variant carriers: 2039
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 5.75e1
  variant carriers: 3039
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 1.75e1
  variant carriers: 1632
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 2.75e1
  variant carriers: 4887
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 2.25e1
  variant carriers: 3263
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 589
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 4.75e1
  variant carriers: 5492
genotype depth: GenotypeDepth
  all individuals: 7725
  bin: 3.75e1
  variant carriers: 6993
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.75e1
  variant carriers: 673
genotype depth: GenotypeDepth
  all individuals: 7047
  bin: 4.25e1
  variant carriers: 6586
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 8.25e1
  variant carriers: 412
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 291
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 8.25e1
  variant carriers: 1410
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.75e1
  variant carriers: 128
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.75e1
  variant carriers: 308
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 198
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 5.75e1
  variant carriers: 448
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 8.75e1
  variant carriers: 790
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.5e0
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.25e1
  variant carriers: 152
genotype quality: GenotypeQuality
  all individuals: 39997
  bin: 9.75e1
  variant carriers: 39228
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.75e1
  variant carriers: 474
num of homozygotes: 26542
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

6-109982165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982165
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982165
    reference: chr 6
allele count: 1
allele frequency: 9.048299824462984e-6
allele num: 110518
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.445-1549A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.108-1549A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.445-1549A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.445-1549A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2319-1549A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.214-1549A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.445-1549A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2368
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/6-109982188-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982188
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982188
    reference: chr 6
allele count: 1
allele frequency: 9.131252625235129e-6
allele num: 109514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.444+1566T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.444+1566T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+1566T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.444+1566T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.444+1566T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2320+1566T>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+1566T>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3257
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-109982197-CACATAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982197
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982191
    reference: chr 6
allele count: 1
allele frequency: 9.187292137515388e-6
allele num: 108846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4894
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4883
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2907
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: CACATAT
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

6-109982203-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109982203
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109982203
    reference: chr 6
allele count: 3
allele frequency: 2.777623465363035e-5
allele num: 108006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.444+1551A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+1551A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+1551A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2320+1551A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.444+1551A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.444+1551A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.444+1551A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5370
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3006
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4360
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5881
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

6-109983705-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109983705
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109983705
    reference: chr 6
allele count: 2
allele frequency: 1.735689242198077e-5
allele num: 115228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.444+49A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2320+49A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+49A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+49A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.444+49A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.444+49A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.444+49A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2498
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

6-109983706-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109983706
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109983706
    reference: chr 6
allele count: 1
allele frequency: 8.681158413778735e-6
allele num: 115192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+48T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.444+48T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2320+48T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.444+48T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.444+48T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+48T>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.444+48T>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9886
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8229
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

6-109983707-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109983707
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109983707
    reference: chr 6
allele count: 1
allele frequency: 8.681459874292461e-6
allele num: 115188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2320+47A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.444+47A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.444+47A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+47A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+47A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.444+47A>G
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.444+47A>G
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29273
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

6-109983707-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109983707
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109983707
    reference: chr 6
allele count: 1
allele frequency: 8.681459874292461e-6
allele num: 115188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+47A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000410186
  ensembl transcript: ENST00000424296
  gene symbol: AK9
  hgvsc: ENST00000424296.2:c.444+47A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000357944
  ensembl transcript: ENST00000368948
  gene symbol: AK9
  hgvsc: ENST00000368948.2:c.444+47A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000344637
  ensembl transcript: ENST00000341338
  gene symbol: AK9
  hgvsc: ENST00000341338.6:c.-2320+47A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000285397
  ensembl transcript: ENST00000285397
  gene symbol: AK9
  hgvsc: ENST00000285397.5:c.444+47A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+47A>C
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000436325
  ensembl transcript: ENST00000532976
  gene symbol: AK9
  hgvsc: ENST00000532976.1:c.444+47A>C
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15264
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29273
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2486
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

6-109983724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 109983724
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 109983724
    reference: chr 6
allele count: 1
allele frequency: 8.635876886939099e-6
allele num: 115796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000407510
  ensembl transcript: ENST00000448084
  gene symbol: AK9
  hgvsc: ENST00000448084.2:c.213+30G>A
  variant of: http://identifiers.org/hgnc/33814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155085
  ensembl protein: ENSP00000431394
  ensembl transcript: ENST00000524674
  gene symbol: AK9
  hgvsc: ENST00000524674.1:c.107+30G>A
  variant of: http://identifiers.org/hgnc/33814
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1080
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6689
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26172
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 178
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3765
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.60570345868525e-5
allele num: 62278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12262
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.942e0

FS
type: SiteQuality
SIO_000300: 1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

DP
type: SiteQuality
SIO_000300: 1.581551e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.375e0

QD
type: SiteQuality
SIO_000300: 1.429e1

VQSLOD
type: SiteQuality
SIO_000300: -4.198e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 5994
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 155
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6782
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 776
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.063131834124201e-4
allele num: 9694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62612
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.822821728034998e-4
allele num: 10972
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

FS
type: SiteQuality
SIO_000300: 5.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.353e1

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 1.595525e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 1
allele frequency: 9.11410864017499e-5
allele num: 10972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.558718861209965e-4
allele num: 8430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

FS
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.595525e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

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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GenotypeQuality
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GenotypeQuality
all individuals: 1952
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GenotypeQuality
all individuals: 1028
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.318516412346381e-5
allele num: 63306
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.442e1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

DP
type: SiteQuality
SIO_000300: 1.633276e6

FS
type: SiteQuality
SIO_000300: 4.003e0

GenotypeQuality
all individuals: 491
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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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variant carriers: 0

GenotypeQuality
all individuals: 1860
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variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596220150683182e-5
allele num: 62648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.184423218221895e-5
allele num: 10888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

DP
type: SiteQuality
SIO_000300: 1.661801e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

FS
type: SiteQuality
SIO_000300: 5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeQuality
all individuals: 2442
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27679
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 696
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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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variant carriers: 8

GenotypeQuality
all individuals: 1062
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variant carriers: 2

GenotypeQuality
all individuals: 626
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variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.673769287288758e-4
allele num: 10888
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.054989816700611e-4
allele num: 9820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.387533875338753e-4
allele num: 14760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.555209953343701e-4
allele num: 6430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.436598135614864e-4
allele num: 62648
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 5.43e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

DP
type: SiteQuality
SIO_000300: 1.661801e6

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 701
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variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.247349382562056e-4
allele num: 16034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.244206662726679e-4
allele num: 64298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.708559046587215e-4
allele num: 11076
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.311084624553039e-3
allele num: 8390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.692e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.575e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

FS
type: SiteQuality
SIO_000300: 1.768e0

DP
type: SiteQuality
SIO_000300: 1.7e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

QD
type: SiteQuality
SIO_000300: 5.54e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2646
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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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11174
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.84251968503937e-5
allele num: 10160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.849e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.709697e6

VQSLOD
type: SiteQuality
SIO_000300: 3.93e-1

QD
type: SiteQuality
SIO_000300: 1.595e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.188495364868077e-4
allele num: 8414
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.723e1

VQSLOD
type: SiteQuality
SIO_000300: -2.448e-1

DP
type: SiteQuality
SIO_000300: 1.742839e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 4.285e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.279e0

GenotypeQuality
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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: 1862
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GenotypeQuality
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GenotypeQuality
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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: 195
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GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65910
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
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: 1
allele frequency: 8.874689385871494e-5
allele num: 11268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.53e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

FS
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

GenotypeQuality
all individuals: 120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3845
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39688
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.034440904263389e-5
allele num: 65910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

QD
type: SiteQuality
SIO_000300: 1.53e1

DP
type: SiteQuality
SIO_000300: 1.767923e6

GenotypeQuality
all individuals: 1888
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2219
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.211937585214361e-4
allele num: 66010
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.257907542579075e-4
allele num: 16440
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.436557231588288e-4
allele num: 11270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.936858415649816e-4
allele num: 10326
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.278145695364238e-4
allele num: 8456
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.99e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

DP
type: SiteQuality
SIO_000300: 1.770736e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
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variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3858
bin: 9.75e1
variant carriers: 20

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.571776897287413e-4
allele num: 6562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.858965272856131e-5
allele num: 11288
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.469794578825817e-4
allele num: 16454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.564525401676299e-5
allele num: 66098
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.93e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

DP
type: SiteQuality
SIO_000300: 1.780103e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.955e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

GenotypeQuality
all individuals: 41293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3848
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1318
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6928
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 3.864734299516908e-4
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
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: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66156
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.781043e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

FS
type: SiteQuality
SIO_000300: 5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

QD
type: SiteQuality
SIO_000300: 1.442e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1892
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3847
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

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

GenotypeQuality
all individuals: 7035
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variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 744
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

DP
type: SiteQuality
SIO_000300: 1.783661e6

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

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

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

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

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 414
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GenotypeQuality
all individuals: 42185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3844
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.517450682852807e-4
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
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: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.063e0

VQSLOD
type: SiteQuality
SIO_000300: -2.047e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 1.784539e6

FS
type: SiteQuality
SIO_000300: 3.575e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 2.021e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 42327
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.831e1

VQSLOD
type: SiteQuality
SIO_000300: -1.896e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.642e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.786901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 737
bin: 9.25e1
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GenotypeQuality
all individuals: 2150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42327
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.13e-1

MQ
type: SiteQuality
SIO_000300: 5.831e1

VQSLOD
type: SiteQuality
SIO_000300: -1.896e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

QD
type: SiteQuality
SIO_000300: 1.068e1

DP
type: SiteQuality
SIO_000300: 1.786901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.642e0

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

GenotypeQuality
all individuals: 188
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3842
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1889
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7058
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 3.965e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.218e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.789121e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

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

European (Finnish)
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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: 11426
num of homozygotes: 0

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

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

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

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

South Asian
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allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.78957e6

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 4.485e0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001741009785676e-5
allele num: 66628
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.234e1

FS
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.591e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.790048e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502070952638214e-5
allele num: 66636
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 2.718e0

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.602e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.99e-1

DP
type: SiteQuality
SIO_000300: 1.790413e6

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
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: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 51
allele frequency: 5.898681471200555e-3
allele num: 8646
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.035e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.145e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.793207e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 1.261e0

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.534e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 1.791474e6

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.46e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

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

South Asian
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allele frequency: 0.0e0
allele num: 16504
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East Asian
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allele frequency: 0.0e0
allele num: 8646
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
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African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66674
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 1
allele frequency: 1.514692517418964e-4
allele num: 6602
num of homozygotes: 0

Other
type: Population
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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 frequency: 0.0e0
allele num: 66676
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African
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East Asian
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South Asian
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MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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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African
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allele num: 10398
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.499790029395885e-5
allele num: 66676
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MQRankSum
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InbreedingCoeff
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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
type: SiteQuality
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66676
num of homozygotes: 0

East Asian
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South Asian
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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QD
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DP
type: SiteQuality
SIO_000300: 1.791649e6

ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: 6.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 1.791575e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6602
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African
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allele frequency: 0.0e0
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Other
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 1.791571e6

MQ
type: SiteQuality
SIO_000300: 5.807e1

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

Latino
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6602
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

FS
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QD
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ClippingRankSum
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SIO_000300: -8.06e-1

BaseQRankSum
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VQSLOD
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SIO_000300: 1.25e0

ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

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

South Asian
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allele count: 6
allele frequency: 3.635482307319437e-4
allele num: 16504
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European (Non-Finnish)
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allele count: 4
allele frequency: 5.998980173370527e-5
allele num: 66678
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East Asian
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allele count: 0
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Other
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.134e0

ReadPosRankSum
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DP
type: SiteQuality
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MQ
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SIO_000300: 5.95e1

BaseQRankSum
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SIO_000300: 1.53e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

QD
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SIO_000300: 9.210000000000001e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 906
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.999850007499625e-5
allele num: 66670
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East Asian
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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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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East Asian
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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FS
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DP
type: SiteQuality
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ClippingRankSum
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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Other
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allele count: 0
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num of homozygotes: 0

African
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allele count: 0
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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DP
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

Other
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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African
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East Asian
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DP
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FS
type: SiteQuality
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QD
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3834
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.931e0

DP
type: SiteQuality
SIO_000300: 1.788995e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

VQSLOD
type: SiteQuality
SIO_000300: -1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: 8.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

GenotypeQuality
all individuals: 1305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 1.92789666473877e-4
allele num: 10374
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.456e1

FS
type: SiteQuality
SIO_000300: 1.456e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.015e0

DP
type: SiteQuality
SIO_000300: 1.788419e6

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.033e0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42601
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 590
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.765778401122019e-5
allele num: 11408
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.929e1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

DP
type: SiteQuality
SIO_000300: 1.786183e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 3.251e0

QD
type: SiteQuality
SIO_000300: 1.192e1

VQSLOD
type: SiteQuality
SIO_000300: 9.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.004e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.353e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

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

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

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42407
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variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7018
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009872381411028e-5
allele num: 66448
num of homozygotes: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

QD
type: SiteQuality
SIO_000300: 8.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.258e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e0

DP
type: SiteQuality
SIO_000300: 1.783508e6

VQSLOD
type: SiteQuality
SIO_000300: -3.015e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7003
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3833
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.519569736961041e-5
allele num: 66378
num of homozygotes: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.581e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.331e0

MQRankSum
type: SiteQuality
SIO_000300: 6.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.422e0

DP
type: SiteQuality
SIO_000300: 1.780717e6

VQSLOD
type: SiteQuality
SIO_000300: -4.135e0

QD
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 1866
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6980
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50779530170984e-5
allele num: 66322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.746e1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

MQRankSum
type: SiteQuality
SIO_000300: -4.34e-1

QD
type: SiteQuality
SIO_000300: 1.514e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.778092e6

FS
type: SiteQuality
SIO_000300: 1.002e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.45e-1

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41997
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variant carriers: 0

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 3834
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.514e1

MQRankSum
type: SiteQuality
SIO_000300: -4.34e-1

FS
type: SiteQuality
SIO_000300: 1.002e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 1.778092e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.45e-1

MQ
type: SiteQuality
SIO_000300: 5.746e1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
all individuals: 41370
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1852
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3912
bin: 9.75e1
variant carriers: 91

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

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

European (Non-Finnish)
type: Population
allele count: 78
allele frequency: 1.179138321995465e-3
allele num: 66150
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.567600487210718e-4
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.64741641337386e-4
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.81057268722467e-5
allele num: 11350
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
type: SiteQuality
SIO_000300: 1.77318e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.969e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

QD
type: SiteQuality
SIO_000300: 1.204e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.77e0

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

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

GenotypeQuality
all individuals: 1852
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2103
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variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 726
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variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 5.609460278956943e-4
allele num: 65960
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.945903872348706e-4
allele num: 10278
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.531696980399082e-4
allele num: 11326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.522533495736906e-4
allele num: 6568
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

QD
type: SiteQuality
SIO_000300: 1.639e1

MQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.757588e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.25e1
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GenotypeQuality
all individuals: 2030
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1032
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.224289911851126e-4
allele num: 16336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.680629e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

FS
type: SiteQuality
SIO_000300: 1.601e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.598e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540879534038029e-5
allele num: 64898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.85e-1

DP
type: SiteQuality
SIO_000300: 1.582001e6

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

FS
type: SiteQuality
SIO_000300: 2.372e0

QD
type: SiteQuality
SIO_000300: 1.556e1

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19573
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5594
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 327
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554871412134217e-5
allele num: 64314
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.523768e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.87e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.634e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.861e0

GenotypeQuality
all individuals: 1918
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5792
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3841
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562793023691942e-5
allele num: 63988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.543e0

DP
type: SiteQuality
SIO_000300: 1.514216e6

MQRankSum
type: SiteQuality
SIO_000300: -1.387e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.463e0

QD
type: SiteQuality
SIO_000300: 7.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

GenotypeQuality
all individuals: 3898
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8039
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.316872427983539e-4
allele num: 60750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.973684210526316e-4
allele num: 15200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.893e0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.352e1

DP
type: SiteQuality
SIO_000300: 1.90825e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

GenotypeQuality
all individuals: 19288
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3898
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.646090534979424e-5
allele num: 60750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.893e0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
SIO_000300: 1.90825e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.352e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3898
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19281
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2082
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3135
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.645657110884376e-5
allele num: 60766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.708e0

DP
type: SiteQuality
SIO_000300: 1.90904e6

QD
type: SiteQuality
SIO_000300: 5.09e0

FS
type: SiteQuality
SIO_000300: 1.292e0

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.464e0

GenotypeQuality
all individuals: 3886
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19284
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4891
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3138
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60762
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.560818790185015e-5
allele num: 15242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.257e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.549e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.915053e6

GenotypeQuality
all individuals: 899
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11400
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.64533219256968e-5
allele num: 60778
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.543e1

DP
type: SiteQuality
SIO_000300: 1.93315e6

FS
type: SiteQuality
SIO_000300: 5.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

GenotypeQuality
all individuals: 11915
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19301
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
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variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5066
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.490977541217708e-5
allele num: 15406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.768e0

DP
type: SiteQuality
SIO_000300: 1.938424e6

QD
type: SiteQuality
SIO_000300: 1.133e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 5.023e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 298
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11956
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
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variant carriers: 0

GenotypeQuality
all individuals: 19349
bin: 9.75e1
variant carriers: 72

GenotypeQuality
all individuals: 2748
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3989
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 8.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 6.078727738713281e-4
allele num: 60868
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 36
allele frequency: 5.504587155963303e-3
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.219512195121951e-3
allele num: 820
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.317e0

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

QD
type: SiteQuality
SIO_000300: 1.298e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.941555e6

GenotypeQuality
all individuals: 664
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 3988
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11977
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.223690651003426e-4
allele num: 8172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15426
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

FS
type: SiteQuality
SIO_000300: 6.176e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.071e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.076e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

DP
type: SiteQuality
SIO_000300: 1.942183e6

QD
type: SiteQuality
SIO_000300: 7.31e0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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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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bin: 3.25e1
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GenotypeQuality
all individuals: 19318
bin: 9.75e1
variant carriers: 12

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2766
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.135137798508688e-4
allele num: 60886
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.06e0

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.867e0

DP
type: SiteQuality
SIO_000300: 1.943633e6

MQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

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

GenotypeQuality
all individuals: 2767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11219
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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: 19315
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 650
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.642629521337758e-5
allele num: 60878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

FS
type: SiteQuality
SIO_000300: 2.986e0

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.944459e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 650
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 701
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5058
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.223391240518718e-4
allele num: 8174
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

FS
type: SiteQuality
SIO_000300: 2.986e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

QD
type: SiteQuality
SIO_000300: 1.009e1

DP
type: SiteQuality
SIO_000300: 1.944459e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.23e-1

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

GenotypeQuality
all individuals: 396
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19316
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 614
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5083
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.642359742477992e-5
allele num: 60888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15490
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.945916e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.092e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.03e-1

FS
type: SiteQuality
SIO_000300: 3.874e0

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 121

GenotypeQuality
all individuals: 162
bin: 2.5e0
variant carriers: 29

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 92

GenotypeQuality
all individuals: 3964
bin: 6.25e1
variant carriers: 897

GenotypeQuality
all individuals: 2101
bin: 6.75e1
variant carriers: 1084

GenotypeQuality
all individuals: 289
bin: 4.25e1
variant carriers: 279

GenotypeQuality
all individuals: 1750
bin: 7.75e1
variant carriers: 1286

GenotypeQuality
all individuals: 1751
bin: 9.25e1
variant carriers: 1504

GenotypeQuality
all individuals: 673
bin: 5.25e1
variant carriers: 644

GenotypeQuality
all individuals: 1003
bin: 7.25e1
variant carriers: 677

East Asian
type: Population
allele count: 6846
allele frequency: 8.387650085763293e-1
allele num: 8162
num of homozygotes: 2866

European (Finnish)
type: Population
allele count: 4499
allele frequency: 6.885521885521886e-1
allele num: 6534
num of homozygotes: 1555

South Asian
type: Population
allele count: 13214
allele frequency: 8.231996012957887e-1
allele num: 16052
num of homozygotes: 5487

African
type: Population
allele count: 2914
allele frequency: 3.601977750309023e-1
allele num: 8090
num of homozygotes: 534

Latino
type: Population
allele count: 8783
allele frequency: 7.839164584077115e-1
allele num: 11204
num of homozygotes: 3426

Other
type: Population
allele count: 583
allele frequency: 7.007211538461539e-1
allele num: 832
num of homozygotes: 197

European (Non-Finnish)
type: Population
allele count: 39034
allele frequency: 6.405316704955694e-1
allele num: 60940
num of homozygotes: 12477

BaseQRankSum
type: SiteQuality
SIO_000300: -2.127e0

FS
type: SiteQuality
SIO_000300: 5.41e-1

DP
type: SiteQuality
SIO_000300: 2.323743e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

QD
type: SiteQuality
SIO_000300: 2.082e1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e0

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.000000000000001e-2

GenotypeQuality
all individuals: 585
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
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GenotypeQuality
all individuals: 2165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1007
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7737
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32279
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variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.249375312343828e-4
allele num: 8004
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60532
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.173e1

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.578388e6

VQSLOD
type: SiteQuality
SIO_000300: -2.802e-1

GenotypeQuality
all individuals: 592
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
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variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
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GenotypeQuality
all individuals: 694
bin: 4.25e1
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GenotypeQuality
all individuals: 24815
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variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.75e1
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GenotypeQuality
all individuals: 2907
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.261352169525732e-4
allele num: 7928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60066
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.252e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.865e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

VQSLOD
type: SiteQuality
SIO_000300: -1.604e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

QD
type: SiteQuality
SIO_000300: 1.463e1

DP
type: SiteQuality
SIO_000300: 1.463262e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.97e-1

GenotypeQuality
all individuals: 5396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.5e0
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GenotypeQuality
all individuals: 203
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variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18529
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variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4527
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.674256630056255e-5
allele num: 59728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15198
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.25e0

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

DP
type: SiteQuality
SIO_000300: 1.387819e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

GenotypeQuality
all individuals: 2903
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 200
bin: 2.5e0
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GenotypeQuality
all individuals: 4621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.819709702062643e-4
allele num: 7854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14980
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 8.481e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

QD
type: SiteQuality
SIO_000300: 1.315e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 1.340417e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 1271
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.119832776963155e-5
allele num: 64106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

QD
type: SiteQuality
SIO_000300: 1.767e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.57097e6

GenotypeQuality
all individuals: 242
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28477
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1812
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560403208188996e-5
allele num: 64086
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e0

MQRankSum
type: SiteQuality
SIO_000300: -1.767e0

VQSLOD
type: SiteQuality
SIO_000300: -1.89e0

DP
type: SiteQuality
SIO_000300: 1.572325e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.852e1

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
all individuals: 251
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2731
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2222
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8205
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.008267795926598e-4
allele num: 9918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14034
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

DP
type: SiteQuality
SIO_000300: 1.574037e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

QD
type: SiteQuality
SIO_000300: 1.862e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.049e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1263
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559965056782728e-5
allele num: 64104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.049e0

DP
type: SiteQuality
SIO_000300: 1.574037e6

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.862e1

MQ
type: SiteQuality
SIO_000300: 6.0e1