8-41577220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577220
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577220
    reference: chr 8
allele count: 5
allele frequency: 4.118548294097296e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1066G>A
  hgvsp: ENSP00000380149.1:p.Val356Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1066G>A
  hgvsp: ENSP00000289734.7:p.Val356Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1066G>A
  hgvsp: ENSP00000380147.1:p.Val356Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1066G>A
  hgvsp: ENSP00000369082.2:p.Val356Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1066G>A
  hgvsp: ENSP00000309131.5:p.Val356Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1066G>A
  hgvsp: ENSP00000339620.4:p.Val356Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1165G>A
  hgvsp: ENSP00000265709.8:p.Val389Ile
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8093
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val389Ile
num of homozygotes: 1
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-41577222-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577222
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577222
    reference: chr 8
allele count: 7
allele frequency: 5.765777638666952e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1064A>G
  hgvsp: ENSP00000380149.1:p.Lys355Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1064A>G
  hgvsp: ENSP00000309131.5:p.Lys355Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1064A>G
  hgvsp: ENSP00000339620.4:p.Lys355Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1064A>G
  hgvsp: ENSP00000369082.2:p.Lys355Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1064A>G
  hgvsp: ENSP00000289734.7:p.Lys355Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1064A>G
  hgvsp: ENSP00000380147.1:p.Lys355Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1163A>G
  hgvsp: ENSP00000265709.8:p.Lys388Arg
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 14734
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21347
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3314
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys388Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-41577225-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577225
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577225
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1061C>G
  hgvsp: ENSP00000289734.7:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1061C>G
  hgvsp: ENSP00000339620.4:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1061C>G
  hgvsp: ENSP00000380149.1:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1061C>G
  hgvsp: ENSP00000369082.2:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1061C>G
  hgvsp: ENSP00000380147.1:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1160C>G
  hgvsp: ENSP00000265709.8:p.Ala387Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1061C>G
  hgvsp: ENSP00000309131.5:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala387Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

8-41577230-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577230
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577230
    reference: chr 8
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1056G>C
  hgvsp: ENSP00000369082.2:p.Arg352Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1155G>C
  hgvsp: ENSP00000265709.8:p.Arg385Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1056G>C
  hgvsp: ENSP00000339620.4:p.Arg352Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1056G>C
  hgvsp: ENSP00000380147.1:p.Arg352Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1056G>C
  hgvsp: ENSP00000380149.1:p.Arg352Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1056G>C
  hgvsp: ENSP00000309131.5:p.Arg352Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1056G>C
  hgvsp: ENSP00000289734.7:p.Arg352Ser
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14726
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg385Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

8-41577232-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577232
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577232
    reference: chr 8
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1054A>G
  hgvsp: ENSP00000380147.1:p.Arg352Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1054A>G
  hgvsp: ENSP00000289734.7:p.Arg352Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1054A>G
  hgvsp: ENSP00000369082.2:p.Arg352Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1054A>G
  hgvsp: ENSP00000309131.5:p.Arg352Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1054A>G
  hgvsp: ENSP00000339620.4:p.Arg352Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1054A>G
  hgvsp: ENSP00000380149.1:p.Arg352Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1153A>G
  hgvsp: ENSP00000265709.8:p.Arg385Gly
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8099
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14725
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg385Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

8-41577257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577257
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577257
    reference: chr 8
allele count: 5
allele frequency: 4.118276912939626e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1029C>T
  hgvsp: ENST00000396942.1:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1029C>T
  hgvsp: ENST00000396945.1:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1128C>T
  hgvsp: ENST00000265709.8:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1029C>T
  hgvsp: ENST00000289734.7:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1029C>T
  hgvsp: ENST00000379758.2:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1029C>T
  hgvsp: ENST00000352337.4:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1029C>T
  hgvsp: ENST00000347528.4:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His376His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-41577260-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577260
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577260
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1026C>T
  hgvsp: ENST00000347528.4:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1026C>T
  hgvsp: ENST00000289734.7:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1026C>T
  hgvsp: ENST00000352337.4:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1026C>T
  hgvsp: ENST00000379758.2:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1125C>T
  hgvsp: ENST00000265709.8:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1026C>T
  hgvsp: ENST00000396945.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1026C>T
  hgvsp: ENST00000396942.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3864
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu375Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

8-41577278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577278
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577278
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1008G>A
  hgvsp: ENST00000347528.4:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1008G>A
  hgvsp: ENST00000396945.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1008G>A
  hgvsp: ENST00000352337.4:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1008G>A
  hgvsp: ENST00000379758.2:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1107G>A
  hgvsp: ENST00000265709.8:c.1107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1008G>A
  hgvsp: ENST00000396942.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1008G>A
  hgvsp: ENST00000289734.7:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu369Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-41577281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577281
    reference: chr 8
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1005C>T
  hgvsp: ENST00000396942.1:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1005C>T
  hgvsp: ENST00000396945.1:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1005C>T
  hgvsp: ENST00000289734.7:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1005C>T
  hgvsp: ENST00000379758.2:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1005C>T
  hgvsp: ENST00000347528.4:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1005C>T
  hgvsp: ENST00000352337.4:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1104C>T
  hgvsp: ENST00000265709.8:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14721
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr368Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-41577281-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577281
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.1005C>G
  hgvsp: ENST00000396942.1:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.1005C>G
  hgvsp: ENST00000352337.4:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.1005C>G
  hgvsp: ENST00000347528.4:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.1005C>G
  hgvsp: ENST00000289734.7:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.1005C>G
  hgvsp: ENST00000379758.2:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.1005C>G
  hgvsp: ENST00000396945.1:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1104C>G
  hgvsp: ENST00000265709.8:c.1104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr368Thr
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

8-41577288-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577288
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577288
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1097A>G
  hgvsp: ENSP00000265709.8:p.Asp366Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.998A>G
  hgvsp: ENSP00000289734.7:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.998A>G
  hgvsp: ENSP00000339620.4:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.998A>G
  hgvsp: ENSP00000369082.2:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.998A>G
  hgvsp: ENSP00000380147.1:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.998A>G
  hgvsp: ENSP00000309131.5:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.998A>G
  hgvsp: ENSP00000380149.1:p.Asp333Gly
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8094
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp366Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-41577289-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577289
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577289
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.997G>T
  hgvsp: ENSP00000380147.1:p.Asp333Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1096G>T
  hgvsp: ENSP00000265709.8:p.Asp366Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.997G>T
  hgvsp: ENSP00000369082.2:p.Asp333Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.997G>T
  hgvsp: ENSP00000380149.1:p.Asp333Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.997G>T
  hgvsp: ENSP00000309131.5:p.Asp333Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.997G>T
  hgvsp: ENSP00000289734.7:p.Asp333Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.997G>T
  hgvsp: ENSP00000339620.4:p.Asp333Tyr
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3858
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4668
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp366Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

8-41577289-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577289
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577289
    reference: chr 8
allele count: 129
allele frequency: 1.062515443538423e-3
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1096G>A
  hgvsp: ENSP00000265709.8:p.Asp366Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.997G>A
  hgvsp: ENSP00000380147.1:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.997G>A
  hgvsp: ENSP00000369082.2:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.997G>A
  hgvsp: ENSP00000309131.5:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.997G>A
  hgvsp: ENSP00000339620.4:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.997G>A
  hgvsp: ENSP00000380149.1:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.997G>A
  hgvsp: ENSP00000289734.7:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 17077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8093
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14735
  bin: 9.75e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp366Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

8-41577290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577290
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577290
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.996C>T
  hgvsp: ENST00000347528.4:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.996C>T
  hgvsp: ENST00000396942.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1095C>T
  hgvsp: ENST00000265709.8:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.996C>T
  hgvsp: ENST00000289734.7:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.996C>T
  hgvsp: ENST00000379758.2:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.996C>T
  hgvsp: ENST00000396945.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.996C>T
  hgvsp: ENST00000352337.4:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp365Asp
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: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

8-41577300-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577300
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577300
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.986C>G
  hgvsp: ENSP00000369082.2:p.Ala329Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.986C>G
  hgvsp: ENSP00000380147.1:p.Ala329Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.986C>G
  hgvsp: ENSP00000339620.4:p.Ala329Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.986C>G
  hgvsp: ENSP00000380149.1:p.Ala329Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.986C>G
  hgvsp: ENSP00000309131.5:p.Ala329Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.986C>G
  hgvsp: ENSP00000289734.7:p.Ala329Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1085C>G
  hgvsp: ENSP00000265709.8:p.Ala362Gly
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15206
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala362Gly
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

8-41577301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577301
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577301
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.985G>A
  hgvsp: ENSP00000380149.1:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1084G>A
  hgvsp: ENSP00000265709.8:p.Ala362Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.985G>A
  hgvsp: ENSP00000309131.5:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.985G>A
  hgvsp: ENSP00000339620.4:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.985G>A
  hgvsp: ENSP00000289734.7:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.985G>A
  hgvsp: ENSP00000369082.2:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.985G>A
  hgvsp: ENSP00000380147.1:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14637
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala362Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

8-41577305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577305
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577305
    reference: chr 8
allele count: 324
allele frequency: 2.668687401159726e-3
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.981C>T
  hgvsp: ENST00000379758.2:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.981C>T
  hgvsp: ENST00000396942.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.981C>T
  hgvsp: ENST00000347528.4:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.981C>T
  hgvsp: ENST00000352337.4:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1080C>T
  hgvsp: ENST00000265709.8:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.981C>T
  hgvsp: ENST00000289734.7:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.981C>T
  hgvsp: ENST00000396945.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4673
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr360Tyr
num of homozygotes: 5
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

8-41577307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577307
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577307
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.979T>C
  hgvsp: ENSP00000339620.4:p.Tyr327His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1078T>C
  hgvsp: ENSP00000265709.8:p.Tyr360His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.979T>C
  hgvsp: ENSP00000289734.7:p.Tyr327His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.979T>C
  hgvsp: ENSP00000380147.1:p.Tyr327His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.979T>C
  hgvsp: ENSP00000309131.5:p.Tyr327His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.979T>C
  hgvsp: ENSP00000369082.2:p.Tyr327His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.979T>C
  hgvsp: ENSP00000380149.1:p.Tyr327His
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2772
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr360His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-41577309-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577309
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577309
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.977A>T
  hgvsp: ENSP00000289734.7:p.Gln326Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.977A>T
  hgvsp: ENSP00000380147.1:p.Gln326Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.977A>T
  hgvsp: ENSP00000380149.1:p.Gln326Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1076A>T
  hgvsp: ENSP00000265709.8:p.Gln359Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.977A>T
  hgvsp: ENSP00000309131.5:p.Gln326Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.977A>T
  hgvsp: ENSP00000339620.4:p.Gln326Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.977A>T
  hgvsp: ENSP00000369082.2:p.Gln326Leu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14407
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln359Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-41577314-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577314
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577314
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.972G>C
  hgvsp: ENST00000347528.4:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1071G>C
  hgvsp: ENST00000265709.8:c.1071G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.972G>C
  hgvsp: ENST00000396942.1:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.972G>C
  hgvsp: ENST00000289734.7:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.972G>C
  hgvsp: ENST00000352337.4:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.972G>C
  hgvsp: ENST00000379758.2:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.972G>C
  hgvsp: ENST00000396945.1:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14406
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu357Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-41577321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577321
    reference: chr 8
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.965G>A
  hgvsp: ENSP00000309131.5:p.Arg322Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.965G>A
  hgvsp: ENSP00000289734.7:p.Arg322Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.965G>A
  hgvsp: ENSP00000369082.2:p.Arg322Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.965G>A
  hgvsp: ENSP00000380147.1:p.Arg322Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.965G>A
  hgvsp: ENSP00000339620.4:p.Arg322Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.965G>A
  hgvsp: ENSP00000380149.1:p.Arg322Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1064G>A
  hgvsp: ENSP00000265709.8:p.Arg355Gln
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2772
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg355Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/8-41577321-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577321
    reference: chr 8
allele count: 21
allele frequency: 1.72970479704797e-4
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.965G>T
  hgvsp: ENSP00000309131.5:p.Arg322Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.965G>T
  hgvsp: ENSP00000369082.2:p.Arg322Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1064G>T
  hgvsp: ENSP00000265709.8:p.Arg355Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.965G>T
  hgvsp: ENSP00000380149.1:p.Arg322Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.965G>T
  hgvsp: ENSP00000289734.7:p.Arg322Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.965G>T
  hgvsp: ENSP00000380147.1:p.Arg322Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.965G>T
  hgvsp: ENSP00000339620.4:p.Arg322Leu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg355Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

8-41577322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577322
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577322
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.964C>T
  hgvsp: ENSP00000289734.7:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.964C>T
  hgvsp: ENSP00000339620.4:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.964C>T
  hgvsp: ENSP00000380147.1:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.964C>T
  hgvsp: ENSP00000309131.5:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.964C>T
  hgvsp: ENSP00000380149.1:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.964C>T
  hgvsp: ENSP00000369082.2:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1063C>T
  hgvsp: ENSP00000265709.8:p.Arg355Trp
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21544
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14393
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg355Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

8-41577327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577327
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577327
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.959G>A
  hgvsp: ENSP00000380147.1:p.Cys320Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.959G>A
  hgvsp: ENSP00000380149.1:p.Cys320Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.959G>A
  hgvsp: ENSP00000339620.4:p.Cys320Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.959G>A
  hgvsp: ENSP00000369082.2:p.Cys320Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1058G>A
  hgvsp: ENSP00000265709.8:p.Cys353Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.959G>A
  hgvsp: ENSP00000309131.5:p.Cys320Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.959G>A
  hgvsp: ENSP00000289734.7:p.Cys320Tyr
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2773
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys353Tyr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-41577330-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577330
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577330
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.956A>C
  hgvsp: ENSP00000289734.7:p.Asp319Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.956A>C
  hgvsp: ENSP00000380147.1:p.Asp319Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.956A>C
  hgvsp: ENSP00000339620.4:p.Asp319Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1055A>C
  hgvsp: ENSP00000265709.8:p.Asp352Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.956A>C
  hgvsp: ENSP00000369082.2:p.Asp319Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.956A>C
  hgvsp: ENSP00000380149.1:p.Asp319Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.956A>C
  hgvsp: ENSP00000309131.5:p.Asp319Ala
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21541
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14394
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp352Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

8-41577331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577331
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577331
    reference: chr 8
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.955G>A
  hgvsp: ENSP00000380147.1:p.Asp319Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.955G>A
  hgvsp: ENSP00000369082.2:p.Asp319Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.955G>A
  hgvsp: ENSP00000309131.5:p.Asp319Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1054G>A
  hgvsp: ENSP00000265709.8:p.Asp352Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.955G>A
  hgvsp: ENSP00000380149.1:p.Asp319Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.955G>A
  hgvsp: ENSP00000289734.7:p.Asp319Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.955G>A
  hgvsp: ENSP00000339620.4:p.Asp319Asn
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2773
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp352Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

8-41577332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577332
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577332
    reference: chr 8
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.954C>T
  hgvsp: ENST00000347528.4:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.954C>T
  hgvsp: ENST00000289734.7:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1053C>T
  hgvsp: ENST00000265709.8:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.954C>T
  hgvsp: ENST00000352337.4:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.954C>T
  hgvsp: ENST00000379758.2:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.954C>T
  hgvsp: ENST00000396945.1:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.954C>T
  hgvsp: ENST00000396942.1:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14392
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu351Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

8-41577339-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577339
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577339
    reference: chr 8
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.947A>G
  hgvsp: ENSP00000339620.4:p.Asp316Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.947A>G
  hgvsp: ENSP00000380147.1:p.Asp316Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.947A>G
  hgvsp: ENSP00000309131.5:p.Asp316Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.947A>G
  hgvsp: ENSP00000289734.7:p.Asp316Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1046A>G
  hgvsp: ENSP00000265709.8:p.Asp349Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.947A>G
  hgvsp: ENSP00000380149.1:p.Asp316Gly
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.947A>G
  hgvsp: ENSP00000369082.2:p.Asp316Gly
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14385
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp349Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-41577350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577350
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577350
    reference: chr 8
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1035G>A
  hgvsp: ENST00000265709.8:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.936G>A
  hgvsp: ENST00000352337.4:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.936G>A
  hgvsp: ENST00000347528.4:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.936G>A
  hgvsp: ENST00000379758.2:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.936G>A
  hgvsp: ENST00000396945.1:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.936G>A
  hgvsp: ENST00000396942.1:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.936G>A
  hgvsp: ENST00000289734.7:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14384
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3876
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala345Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

8-41577361-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577361
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577361
    reference: chr 8
allele count: 6
allele frequency: 4.942502224126001e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.925A>G
  hgvsp: ENSP00000289734.7:p.Ile309Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.925A>G
  hgvsp: ENSP00000369082.2:p.Ile309Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.925A>G
  hgvsp: ENSP00000380147.1:p.Ile309Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.925A>G
  hgvsp: ENSP00000339620.4:p.Ile309Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.925A>G
  hgvsp: ENSP00000309131.5:p.Ile309Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1024A>G
  hgvsp: ENSP00000265709.8:p.Ile342Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.925A>G
  hgvsp: ENSP00000380149.1:p.Ile309Val
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8142
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21551
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile342Val
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

8-41577365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577365
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577365
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1020C>T
  hgvsp: ENST00000265709.8:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.921C>T
  hgvsp: ENST00000289734.7:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.921C>T
  hgvsp: ENST00000352337.4:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.921C>T
  hgvsp: ENST00000347528.4:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.921C>T
  hgvsp: ENST00000379758.2:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.921C>T
  hgvsp: ENST00000396942.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.921C>T
  hgvsp: ENST00000396945.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21546
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3876
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser340Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

8-41577366-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577366
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577366
    reference: chr 8
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.920C>A
  hgvsp: ENSP00000369082.2:p.Ser307Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.920C>A
  hgvsp: ENSP00000380147.1:p.Ser307Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.920C>A
  hgvsp: ENSP00000339620.4:p.Ser307Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.920C>A
  hgvsp: ENSP00000289734.7:p.Ser307Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.920C>A
  hgvsp: ENSP00000309131.5:p.Ser307Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.920C>A
  hgvsp: ENSP00000380149.1:p.Ser307Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1019C>A
  hgvsp: ENSP00000265709.8:p.Ser340Tyr
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser340Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-41577373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577373
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577373
    reference: chr 8
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.913G>A
  hgvsp: ENSP00000369082.2:p.Gly305Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.913G>A
  hgvsp: ENSP00000289734.7:p.Gly305Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1012G>A
  hgvsp: ENSP00000265709.8:p.Gly338Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.913G>A
  hgvsp: ENSP00000380149.1:p.Gly305Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.913G>A
  hgvsp: ENSP00000380147.1:p.Gly305Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.913G>A
  hgvsp: ENSP00000309131.5:p.Gly305Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.913G>A
  hgvsp: ENSP00000339620.4:p.Gly305Ser
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3873
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly338Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

8-41577374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577374
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577374
    reference: chr 8
allele count: 4
allele frequency: 3.29663084327817e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.912C>T
  hgvsp: ENST00000379758.2:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.912C>T
  hgvsp: ENST00000289734.7:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1011C>T
  hgvsp: ENST00000265709.8:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.912C>T
  hgvsp: ENST00000347528.4:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.912C>T
  hgvsp: ENST00000352337.4:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.912C>T
  hgvsp: ENST00000396945.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.912C>T
  hgvsp: ENST00000396942.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1011C>T
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-41577381-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577381
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577381
    reference: chr 8
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-5C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-5C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-5C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-5C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-5C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-5C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-5C>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2775
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1009-5C>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum

8-41577387-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577387
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577387
    reference: chr 8
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-11T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-11T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-11T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-11T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-11T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-11T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-11T>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8078
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-41577394-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577394
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577394
    reference: chr 8
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-18G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-18G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-18G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-18G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-18G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-18G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-18G>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14353
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

8-41577402-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577402
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577402
    reference: chr 8
allele count: 8
allele frequency: 6.619338397127208e-5
allele num: 120858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-26T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-26T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-26T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-26T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-26T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-26T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-26T>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3168
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14347
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20407
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

8-41577412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577412
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577412
    reference: chr 8
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-36G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-36G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-36G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-36G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-36G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-36G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-36G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6938
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4462
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-41577423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577423
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577423
    reference: chr 8
allele count: 1
allele frequency: 8.34599142032082e-6
allele num: 119818
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-47G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-47G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-47G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-47G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-47G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-47G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-47G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10717
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5983
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14316
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

8-41577424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577424
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577424
    reference: chr 8
allele count: 22
allele frequency: 1.837897445322551e-4
allele num: 119702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-48C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-48C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-48C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-48C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-48C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-48C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-48C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9664
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10808
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9521
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

8-41577425-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577425
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577425
    reference: chr 8
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-49T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-49T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-49T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-49T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-49T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-49T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-49T>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4292
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3706
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

8-41577428-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41577428
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41577428
    reference: chr 8
allele count: 31
allele frequency: 2.594142259414226e-4
allele num: 119500
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1009-52T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.910-52T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.910-52T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.910-52T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.910-52T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.910-52T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.910-52T>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10581
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14332
  bin: 9.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 3687
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2613
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2046
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/8-41580596-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580596
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580596
    reference: chr 8
allele count: 60
allele frequency: 4.950413359515519e-4
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+47G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+47G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+47G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+47G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+47G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+47G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+47G>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9838
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10095
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4663
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3258
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-41580601-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580601
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580601
    reference: chr 8
allele count: 20
allele frequency: 1.649702228747711e-4
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+42C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+42C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+42C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+42C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+42C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+42C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+42C>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8212
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9903
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3663
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-41580602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580602
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580602
    reference: chr 8
allele count: 10
allele frequency: 8.247694769311977e-5
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+41G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+41G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+41G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+41G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+41G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+41G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+41G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9917
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30086
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-41580605-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580605
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580605
    reference: chr 8
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+38A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+38A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+38A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+38A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+38A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+38A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+38A>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4713
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

8-41580606-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580606
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580606
    reference: chr 8
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+37C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+37C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+37C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+37C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+37C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+37C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+37C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30109
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

8-41580607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580607
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580607
    reference: chr 8
allele count: 40851
allele frequency: 3.375334633307995e-1
allele num: 121028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+36A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+36A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+36A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+36A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+36A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+36A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+36A>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 6.75e1
  variant carriers: 1594
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 8.25e1
  variant carriers: 621
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.25e1
  variant carriers: 2188
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 1171
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 5.25e1
  variant carriers: 3615
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 4.75e1
  variant carriers: 3970
genotype depth: GenotypeDepth
  all individuals: 6550
  bin: 9.75e1
  variant carriers: 4642
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 2855
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 2.25e1
  variant carriers: 518
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 2.75e1
  variant carriers: 1259
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 4.25e1
  variant carriers: 3814
genotype depth: GenotypeDepth
  all individuals: 8070
  bin: 3.25e1
  variant carriers: 2219
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.75e1
  variant carriers: 848
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 8.75e1
  variant carriers: 546
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.25e1
  variant carriers: 427
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 3.75e1
  variant carriers: 3215
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 40695
  bin: 9.75e1
  variant carriers: 32758
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3261
  bin: 6.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 100
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 9.25e1
  variant carriers: 191
num of homozygotes: 7203
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

8-41580616-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580616
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580616
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+27A>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+27A>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+27A>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+27A>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+27A>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+27A>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+27A>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12917
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15811
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6938
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3760
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4481
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

8-41580616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580616
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580616
    reference: chr 8
allele count: 6
allele frequency: 4.943479550472926e-5
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+27A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+27A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+27A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+27A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+27A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+27A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+27A>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4481
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-41580617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580617
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580617
    reference: chr 8
allele count: 3
allele frequency: 2.471699045924168e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+26C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+26C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+26C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+26C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+26C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+26C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+26C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21746
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15809
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-41580618-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580618
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580618
    reference: chr 8
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+25G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+25G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+25G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+25G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+25G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+25G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+25G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12964
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2860
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15797
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-41580619-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580619
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580619
    reference: chr 8
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+24C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+24C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+24C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+24C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+24C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+24C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+24C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4474
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15941
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21718
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

8-41580631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580631
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580631
    reference: chr 8
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+12C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+12C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+12C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+12C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+12C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+12C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+12C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16118
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21712
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-41580632-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580632
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580632
    reference: chr 8
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+11C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+11C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+11C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+11C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+11C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+11C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+11C>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2866
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

8-41580634-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580634
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580634
    reference: chr 8
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+9T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+9T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+9T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+9T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+9T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+9T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+9T>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7786
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6926
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2964
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3745
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

8-41580636-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580636
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580636
    reference: chr 8
allele count: 5420
allele frequency: 4.464800566749592e-2
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+7A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+7A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+7A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+7A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+7A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+7A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+7A>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 4.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 6.75e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13877
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.75e1
  variant carriers: 257
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 436
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.75e1
  variant carriers: 420
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.25e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 3.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 8.75e1
  variant carriers: 394
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 4.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.25e1
  variant carriers: 436
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 9.75e1
  variant carriers: 1802
genotype depth: GenotypeDepth
  all individuals: 12699
  bin: 3.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.25e1
  variant carriers: 302
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22287
  bin: 9.75e1
  variant carriers: 5253
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1008+7A>G
num of homozygotes: 166
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

8-41580640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580640
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580640
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.909+3G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.909+3G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.909+3G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.1008+3G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.909+3G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.909+3G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.909+3G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7523
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4864
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1008+3G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-41580669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580669
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580669
    reference: chr 8
allele count: 5
allele frequency: 4.11820907323823e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.883G>A
  hgvsp: ENSP00000309131.5:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.883G>A
  hgvsp: ENSP00000339620.4:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.883G>A
  hgvsp: ENSP00000380147.1:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.883G>A
  hgvsp: ENSP00000289734.7:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.883G>A
  hgvsp: ENSP00000369082.2:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.982G>A
  hgvsp: ENSP00000265709.8:p.Gly328Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.883G>A
  hgvsp: ENSP00000380149.1:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18361
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Gly328Arg
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-41580670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580670
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580670
    reference: chr 8
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.882C>T
  hgvsp: ENST00000396942.1:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.882C>T
  hgvsp: ENST00000379758.2:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.981C>T
  hgvsp: ENST00000265709.8:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.882C>T
  hgvsp: ENST00000396945.1:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.882C>T
  hgvsp: ENST00000289734.7:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.882C>T
  hgvsp: ENST00000352337.4:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.882C>T
  hgvsp: ENST00000347528.4:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18355
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His327His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

8-41580672-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580672
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580672
    reference: chr 8
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.880C>A
  hgvsp: ENSP00000339620.4:p.His294Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.979C>A
  hgvsp: ENSP00000265709.8:p.His327Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.880C>A
  hgvsp: ENSP00000289734.7:p.His294Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.880C>A
  hgvsp: ENSP00000380149.1:p.His294Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.880C>A
  hgvsp: ENSP00000380147.1:p.His294Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.880C>A
  hgvsp: ENSP00000369082.2:p.His294Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.880C>A
  hgvsp: ENSP00000309131.5:p.His294Asn
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18354
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4012
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17741
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7528
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His327Asn
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

8-41580676-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580676
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580676
    reference: chr 8
allele count: 51
allele frequency: 4.200573254702995e-4
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.876G>A
  hgvsp: ENST00000289734.7:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.876G>A
  hgvsp: ENST00000396942.1:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.876G>A
  hgvsp: ENST00000379758.2:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.876G>A
  hgvsp: ENST00000352337.4:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.975G>A
  hgvsp: ENST00000265709.8:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.876G>A
  hgvsp: ENST00000347528.4:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.876G>A
  hgvsp: ENST00000396945.1:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18373
  bin: 9.75e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4010
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu325Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-41580688-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580688
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580688
    reference: chr 8
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.864A>G
  hgvsp: ENST00000396945.1:c.864A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.963A>G
  hgvsp: ENST00000265709.8:c.963A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.864A>G
  hgvsp: ENST00000396942.1:c.864A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.864A>G
  hgvsp: ENST00000347528.4:c.864A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.864A>G
  hgvsp: ENST00000379758.2:c.864A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.864A>G
  hgvsp: ENST00000352337.4:c.864A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.864A>G
  hgvsp: ENST00000289734.7:c.864A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17751
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser321Ser
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

8-41580691-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580691
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580691
    reference: chr 8
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.861C>G
  hgvsp: ENSP00000380147.1:p.Ile287Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.861C>G
  hgvsp: ENSP00000369082.2:p.Ile287Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.960C>G
  hgvsp: ENSP00000265709.8:p.Ile320Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.861C>G
  hgvsp: ENSP00000339620.4:p.Ile287Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.861C>G
  hgvsp: ENSP00000309131.5:p.Ile287Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.861C>G
  hgvsp: ENSP00000380149.1:p.Ile287Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.861C>G
  hgvsp: ENSP00000289734.7:p.Ile287Met
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4872
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18338
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile320Met
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

8-41580695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580695
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580695
    reference: chr 8
allele count: 12
allele frequency: 9.883864591055103e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.857G>A
  hgvsp: ENSP00000309131.5:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.857G>A
  hgvsp: ENSP00000380147.1:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.857G>A
  hgvsp: ENSP00000369082.2:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.857G>A
  hgvsp: ENSP00000289734.7:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.857G>A
  hgvsp: ENSP00000339620.4:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.956G>A
  hgvsp: ENSP00000265709.8:p.Arg319Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.857G>A
  hgvsp: ENSP00000380149.1:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17748
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4872
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg319Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-41580699-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580699
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580699
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.853G>T
  hgvsp: ENSP00000380147.1:p.Val285Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.853G>T
  hgvsp: ENSP00000369082.2:p.Val285Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.853G>T
  hgvsp: ENSP00000380149.1:p.Val285Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.853G>T
  hgvsp: ENSP00000289734.7:p.Val285Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.853G>T
  hgvsp: ENSP00000339620.4:p.Val285Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.853G>T
  hgvsp: ENSP00000309131.5:p.Val285Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.952G>T
  hgvsp: ENSP00000265709.8:p.Val318Leu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18331
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17759
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4017
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val318Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

8-41580699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580699
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580699
    reference: chr 8
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.853G>A
  hgvsp: ENSP00000289734.7:p.Val285Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.853G>A
  hgvsp: ENSP00000339620.4:p.Val285Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.853G>A
  hgvsp: ENSP00000309131.5:p.Val285Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.853G>A
  hgvsp: ENSP00000380149.1:p.Val285Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.853G>A
  hgvsp: ENSP00000380147.1:p.Val285Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.853G>A
  hgvsp: ENSP00000369082.2:p.Val285Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.952G>A
  hgvsp: ENSP00000265709.8:p.Val318Met
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4870
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7533
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val318Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

8-41580700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580700
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580700
    reference: chr 8
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.852C>T
  hgvsp: ENST00000396945.1:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.852C>T
  hgvsp: ENST00000347528.4:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.852C>T
  hgvsp: ENST00000396942.1:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.852C>T
  hgvsp: ENST00000379758.2:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.951C>T
  hgvsp: ENST00000265709.8:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.852C>T
  hgvsp: ENST00000352337.4:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.852C>T
  hgvsp: ENST00000289734.7:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7533
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His317His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

8-41580701-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580701
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580701
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.851A>G
  hgvsp: ENSP00000339620.4:p.His284Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.950A>G
  hgvsp: ENSP00000265709.8:p.His317Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.851A>G
  hgvsp: ENSP00000369082.2:p.His284Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.851A>G
  hgvsp: ENSP00000289734.7:p.His284Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.851A>G
  hgvsp: ENSP00000380147.1:p.His284Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.851A>G
  hgvsp: ENSP00000309131.5:p.His284Arg
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.851A>G
  hgvsp: ENSP00000380149.1:p.His284Arg
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18329
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4018
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His317Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

8-41580703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580703
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580703
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.849G>A
  hgvsp: ENST00000396942.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.849G>A
  hgvsp: ENST00000396945.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.849G>A
  hgvsp: ENST00000347528.4:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.849G>A
  hgvsp: ENST00000289734.7:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.849G>A
  hgvsp: ENST00000379758.2:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.948G>A
  hgvsp: ENST00000265709.8:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.849G>A
  hgvsp: ENST00000352337.4:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly316Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-41580706-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41580706
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41580706
    reference: chr 8
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.846T>C
  hgvsp: ENST00000347528.4:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.846T>C
  hgvsp: ENST00000379758.2:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.846T>C
  hgvsp: ENST00000352337.4:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.846T>C
  hgvsp: ENST00000289734.7:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.846T>C
  hgvsp: ENST00000396942.1:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.945T>C
  hgvsp: ENST00000265709.8:c.945T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.846T>C
  hgvsp: ENST00000396945.1:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn315Asn
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21344
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 1

MQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

QD
type: SiteQuality
SIO_000300: 1.877e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.619e-1

FS
type: SiteQuality
SIO_000300: 1.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.642e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.444e0

DP
type: SiteQuality
SIO_000300: 2.269088e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 7
allele frequency: 8.088745088976196e-4
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

DP
type: SiteQuality
SIO_000300: 2.269544e6

QD
type: SiteQuality
SIO_000300: 1.241e1

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2752
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.0664e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

DP
type: SiteQuality
SIO_000300: 2.268026e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.459e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.87e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.352e1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 4.952e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.268081e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeQuality
all individuals: 2753
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21360
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.189e0

QD
type: SiteQuality
SIO_000300: 1.206e1

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 2.267951e6

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.85e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

DP
type: SiteQuality
SIO_000300: 2.267994e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

Other
type: Population
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allele num: 908
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.396e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.539e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ReadPosRankSum
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SIO_000300: 8.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 2.267451e6

MQRankSum
type: SiteQuality
SIO_000300: -1.169e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.746e0

VQSLOD
type: SiteQuality
SIO_000300: -3.97e-2

MQRankSum
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SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.052e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 5.613e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.442e1

DP
type: SiteQuality
SIO_000300: 2.267381e6

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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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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African
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East Asian
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Latino
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DP
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FS
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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VQSLOD
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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Other
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Latino
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East Asian
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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African
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South Asian
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East Asian
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DP
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ClippingRankSum
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MQ
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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BaseQRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Other
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MQRankSum
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QD
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DP
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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South Asian
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Latino
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African
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European (Non-Finnish)
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.452e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ReadPosRankSum
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SIO_000300: -1.016e0

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

Other
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South 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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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.991e1

ClippingRankSum
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SIO_000300: 8.63e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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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: 8.637070305752289e-5
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num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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African
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European (Non-Finnish)
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allele num: 66736
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Other
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.141e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

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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East Asian
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European (Non-Finnish)
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allele frequency: 2.547350755214577e-4
allele num: 66736
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Latino
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allele num: 11578
num of homozygotes: 0

South Asian
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African
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European (Finnish)
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Other
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.141e0

InbreedingCoeff
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DP
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ReadPosRankSum
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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SIO_000300: 2.2e-1

MQ
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SIO_000300: 5.967e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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Other
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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DP
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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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 num: 66736
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South Asian
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European (Finnish)
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Latino
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Other
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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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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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Other
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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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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Latino
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num of homozygotes: 0

South Asian
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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FS
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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East Asian
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Other
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
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ClippingRankSum
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SIO_000300: 5.639999999999999e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.009e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.047e0

FS
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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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 count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

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

ReadPosRankSum
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SIO_000300: -6.6e-2

FS
type: SiteQuality
SIO_000300: 6.73e-1

QD
type: SiteQuality
SIO_000300: 1.404e1

InbreedingCoeff
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DP
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SIO_000300: 2.230176e6

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e0

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

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

QD
type: SiteQuality
SIO_000300: 1.109e1

DP
type: SiteQuality
SIO_000300: 2.229558e6

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.118e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 5.396e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.146e0

DP
type: SiteQuality
SIO_000300: 2.229334e6

QD
type: SiteQuality
SIO_000300: 9.41e0

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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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.272e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.228369e6

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.798e0

MQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.14e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.1e0

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

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
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Other
type: Population
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66618
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

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

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.688e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.924e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 8.42e0

DP
type: SiteQuality
SIO_000300: 2.203814e6

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

GenotypeQuality
all individuals: 2756
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 1899
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variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4559
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.751543209876543e-4
allele num: 10368
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.471e1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 2.192021e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

GenotypeQuality
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2742
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GenotypeQuality
all individuals: 246
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50934283213089e-5
allele num: 66254
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.324e0

MQRankSum
type: SiteQuality
SIO_000300: -1.899e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.022e1

DP
type: SiteQuality
SIO_000300: 2.135612e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.039e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.12e-1

GenotypeQuality
all individuals: 1758
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
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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
all individuals: 2719
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520542529574552e-5
allele num: 65766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.201e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 2.066769e6

MQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.43e0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 22

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5836
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GenotypeQuality
all individuals: 2718
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.820167455405897e-4
allele num: 16482
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.673920321392702e-4
allele num: 65714
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.480919649205973e-4
allele num: 8438
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.418e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.24e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

DP
type: SiteQuality
SIO_000300: 2.059725e6

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

GenotypeQuality
all individuals: 2024
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14313
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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: 9903
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3186
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variant carriers: 0

GenotypeQuality
all individuals: 2720
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520588771972508e-5
allele num: 65764
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.184e0

MQRankSum
type: SiteQuality
SIO_000300: -1.184e0

VQSLOD
type: SiteQuality
SIO_000300: -4.204e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.058627e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeQuality
all individuals: 5403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4255
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variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65582
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

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

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

African
type: Population
allele count: 31
allele frequency: 3.012048192771084e-3
allele num: 10292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.052915e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

FS
type: SiteQuality
SIO_000300: 1.498e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

QD
type: SiteQuality
SIO_000300: 1.409e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30086
bin: 9.75e1
variant carriers: 60

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

East Asian
type: Population
allele count: 56
allele frequency: 6.505576208178439e-3
allele num: 8608
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819284414796847e-4
allele num: 16490
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: 11548
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 2.066e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.002e0

DP
type: SiteQuality
SIO_000300: 2.811769e6

QD
type: SiteQuality
SIO_000300: 1.442e1

GenotypeQuality
all individuals: 4689
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
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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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variant carriers: 19

GenotypeQuality
all individuals: 309
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variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 2.999490086685263e-4
allele num: 66678
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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: 6606
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.341e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

FS
type: SiteQuality
SIO_000300: 1.151e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

DP
type: SiteQuality
SIO_000300: 2.816216e6

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
all individuals: 3298
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.886836027713626e-4
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.99847026005579e-5
allele num: 66678
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

DP
type: SiteQuality
SIO_000300: 2.81723e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.206e0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2541
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GenotypeQuality
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 66696
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.820244e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

QD
type: SiteQuality
SIO_000300: 1.545e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.386e0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9591
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3699
bin: 8.25e1
variant carriers: 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: 16496
num of homozygotes: 0

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

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

African
type: Population
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: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.836e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.311e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.966e0

QD
type: SiteQuality
SIO_000300: 1.335e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 2.821145e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.99e0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1897
bin: 8.25e1
variant carriers: 152

GenotypeQuality
all individuals: 2239
bin: 7.75e1
variant carriers: 117

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 25

GenotypeQuality
all individuals: 78
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 12

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 36

GenotypeQuality
all individuals: 1544
bin: 7.25e1
variant carriers: 67

GenotypeQuality
all individuals: 7545
bin: 6.25e1
variant carriers: 55

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 7

Other
type: Population
allele count: 330
allele frequency: 3.634361233480176e-1
allele num: 908
num of homozygotes: 58

European (Non-Finnish)
type: Population
allele count: 23692
allele frequency: 3.560458056565778e-1
allele num: 66542
num of homozygotes: 4222

African
type: Population
allele count: 5276
allele frequency: 5.078937235271467e-1
allele num: 10388
num of homozygotes: 1329

South Asian
type: Population
allele count: 5031
allele frequency: 3.050939963614312e-1
allele num: 16490
num of homozygotes: 786

Latino
type: Population
allele count: 2610
allele frequency: 2.264052741151978e-1
allele num: 11528
num of homozygotes: 312

European (Finnish)
type: Population
allele count: 1919
allele frequency: 2.915527195381343e-1
allele num: 6582
num of homozygotes: 266

East Asian
type: Population
allele count: 1993
allele frequency: 2.320139697322468e-1
allele num: 8590
num of homozygotes: 230

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 2.089e1

DP
type: SiteQuality
SIO_000300: 3.238037e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.13e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

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

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21746
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.421e0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 2.664047e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

QD
type: SiteQuality
SIO_000300: 1.646e1

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

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

GenotypeQuality
all individuals: 6938
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21746
bin: 9.75e1
variant carriers: 6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.184929139301763e-4
allele num: 11572
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.646e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 2.664047e6

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeQuality
all individuals: 4484
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6934
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3758
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.709e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 2.306e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 1.528e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.406e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.664239e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

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

GenotypeQuality
all individuals: 2974
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21722
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 6893
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.818181818181818e-4
allele num: 16500
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.188e1

DP
type: SiteQuality
SIO_000300: 2.665649e6

FS
type: SiteQuality
SIO_000300: 1.446e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.474e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2866
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2972
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.321e1

FS
type: SiteQuality
SIO_000300: 1.041e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

DP
type: SiteQuality
SIO_000300: 2.664602e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4467
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.178e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

QD
type: SiteQuality
SIO_000300: 3.066e1

MQRankSum
type: SiteQuality
SIO_000300: -4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.031e0

DP
type: SiteQuality
SIO_000300: 2.665543e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21713
bin: 9.75e1
variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.665652e6

FS
type: SiteQuality
SIO_000300: 4.867e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.702e0

QD
type: SiteQuality
SIO_000300: 1.326e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

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

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 2865
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 21712
bin: 9.75e1
variant carriers: 4

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993586862057598e-5
allele num: 66738
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.665736e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.402e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 1.474e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2714
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 1

European (Finnish)
type: Population
allele count: 503
allele frequency: 7.605080133051104e-2
allele num: 6614
num of homozygotes: 13

European (Non-Finnish)
type: Population
allele count: 3542
allele frequency: 5.307321166352003e-2
allele num: 66738
num of homozygotes: 108

South Asian
type: Population
allele count: 231
allele frequency: 1.399321541070996e-2
allele num: 16508
num of homozygotes: 6

Other
type: Population
allele count: 43
allele frequency: 4.73568281938326e-2
allele num: 908
num of homozygotes: 1

East Asian
type: Population
allele count: 14
allele frequency: 1.618122977346278e-3
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 871
allele frequency: 7.526788800553059e-2
allele num: 11572
num of homozygotes: 35

African
type: Population
allele count: 216
allele frequency: 2.07652374543357e-2
allele num: 10402
num of homozygotes: 3

DP
type: SiteQuality
SIO_000300: 2.843388e6

QD
type: SiteQuality
SIO_000300: 1.536e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

FS
type: SiteQuality
SIO_000300: 6.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 17721
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.561933e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.119e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4865
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.794e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 2.562325e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

GenotypeQuality
all individuals: 17741
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1974
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3233
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4865
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.561893e6

VQSLOD
type: SiteQuality
SIO_000300: 8.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

FS
type: SiteQuality
SIO_000300: 4.158e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 1.112e1

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

GenotypeQuality
all individuals: 4865
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2996
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variant carriers: 0

GenotypeQuality
all individuals: 3233
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variant carriers: 0

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

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.21e-1

DP
type: SiteQuality
SIO_000300: 2.561886e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.727e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

VQSLOD
type: SiteQuality
SIO_000300: -2.645e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

QD
type: SiteQuality
SIO_000300: 4.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 6.592747977225053e-4
allele num: 66740
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

QD
type: SiteQuality
SIO_000300: 1.232e1

FS
type: SiteQuality
SIO_000300: 1.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.28e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.782e0

DP
type: SiteQuality
SIO_000300: 2.566031e6

GenotypeQuality
all individuals: 0
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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
all individuals: 18337
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.096e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.801e0

VQSLOD
type: SiteQuality
SIO_000300: -1.615e0

MQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

FS
type: SiteQuality
SIO_000300: 1.2291e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

DP
type: SiteQuality
SIO_000300: 2.56155e6

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

GenotypeQuality
all individuals: 4015
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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: 1974
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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: 0
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.12e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

DP
type: SiteQuality
SIO_000300: 2.561577e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

FS
type: SiteQuality
SIO_000300: 5.72e-1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1973
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
all individuals: 7534
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GenotypeQuality
all individuals: 4015
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 10
allele frequency: 1.155535012710885e-3
allele num: 8654
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

DP
type: SiteQuality
SIO_000300: 2.562429e6

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.237e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

GenotypeQuality
all individuals: 7533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

DP
type: SiteQuality
SIO_000300: 2.561619e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.561619e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

DP
type: SiteQuality
SIO_000300: 2.561316e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.035e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 2.561123e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.43e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

East Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.791e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 7.78e-1

InbreedingCoeff
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.127e1

MQRankSum
type: SiteQuality
SIO_000300: -4.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.561136e6