8-41548020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548020
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548020
    reference: chr 8
allele count: 6
allele frequency: 4.952865232537022e-5
allele num: 121142
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.3956G>A
  hgvsp: ENSP00000380149.1:p.Arg1319Gln
  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.3956G>A
  hgvsp: ENSP00000309131.5:p.Arg1319Gln
  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.3956G>A
  hgvsp: ENSP00000380147.1:p.Arg1319Gln
  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.3956G>A
  hgvsp: ENSP00000289734.7:p.Arg1319Gln
  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.3956G>A
  hgvsp: ENSP00000339620.4:p.Arg1319Gln
  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.4079G>A
  hgvsp: ENSP00000265709.8:p.Arg1360Gln
  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.3956G>A
  hgvsp: ENSP00000369082.2:p.Arg1319Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1439G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1920G>A
  hgvsp: ENSP00000430174.1:p.Arg641Gln
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1360Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-41548021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548021
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548021
    reference: chr 8
allele count: 23
allele frequency: 1.898755077105967e-4
allele num: 121132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1438C>T
  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.3955C>T
  hgvsp: ENSP00000380149.1:p.Arg1319Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1919C>T
  hgvsp: ENSP00000430174.1:p.Arg641Trp
  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.3955C>T
  hgvsp: ENSP00000309131.5:p.Arg1319Trp
  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.3955C>T
  hgvsp: ENSP00000380147.1:p.Arg1319Trp
  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.3955C>T
  hgvsp: ENSP00000339620.4:p.Arg1319Trp
  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.3955C>T
  hgvsp: ENSP00000369082.2:p.Arg1319Trp
  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.3955C>T
  hgvsp: ENSP00000289734.7:p.Arg1319Trp
  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.4078C>T
  hgvsp: ENSP00000265709.8:p.Arg1360Trp
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4949
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg1360Trp
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-41548035-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548035
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548035
    reference: chr 8
allele count: 2
allele frequency: 1.652046059044126e-5
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3941A>C
  hgvsp: ENSP00000380147.1:p.His1314Pro
  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.3941A>C
  hgvsp: ENSP00000380149.1:p.His1314Pro
  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.4064A>C
  hgvsp: ENSP00000265709.8:p.His1355Pro
  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.3941A>C
  hgvsp: ENSP00000369082.2:p.His1314Pro
  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.3941A>C
  hgvsp: ENSP00000309131.5:p.His1314Pro
  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.3941A>C
  hgvsp: ENSP00000339620.4:p.His1314Pro
  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.3941A>C
  hgvsp: ENSP00000289734.7:p.His1314Pro
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1424A>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1905A>C
  hgvsp: ENSP00000430174.1:p.His636Pro
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His1355Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-41548044-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548044
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548044
    reference: chr 8
allele count: 6
allele frequency: 4.95785820525533e-5
allele num: 121020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1415G>A
  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.3932G>A
  hgvsp: ENSP00000309131.5:p.Arg1311Gln
  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.3932G>A
  hgvsp: ENSP00000289734.7:p.Arg1311Gln
  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.3932G>A
  hgvsp: ENSP00000380147.1:p.Arg1311Gln
  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.3932G>A
  hgvsp: ENSP00000339620.4:p.Arg1311Gln
  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.3932G>A
  hgvsp: ENSP00000369082.2:p.Arg1311Gln
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1896G>A
  hgvsp: ENSP00000430174.1:p.Arg633Gln
  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.3932G>A
  hgvsp: ENSP00000380149.1:p.Arg1311Gln
  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.4055G>A
  hgvsp: ENSP00000265709.8:p.Arg1352Gln
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2481
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1352Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

8-41548045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548045
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548045
    reference: chr 8
allele count: 5
allele frequency: 4.131616784280024e-5
allele num: 121018
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.3931C>T
  hgvsp: ENSP00000309131.5:p.Arg1311Trp
  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.3931C>T
  hgvsp: ENSP00000380149.1:p.Arg1311Trp
  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.3931C>T
  hgvsp: ENSP00000369082.2:p.Arg1311Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1414C>T
  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.3931C>T
  hgvsp: ENSP00000380147.1:p.Arg1311Trp
  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.3931C>T
  hgvsp: ENSP00000289734.7:p.Arg1311Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1895C>T
  hgvsp: ENSP00000430174.1:p.Arg633Trp
  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.4054C>T
  hgvsp: ENSP00000265709.8:p.Arg1352Trp
  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.3931C>T
  hgvsp: ENSP00000339620.4:p.Arg1311Trp
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg1352Trp
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-41548061-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548061
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548061
    reference: chr 8
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
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.3915G>T
  hgvsp: ENSP00000289734.7:p.Lys1305Asn
  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.3915G>T
  hgvsp: ENSP00000380147.1:p.Lys1305Asn
  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.3915G>T
  hgvsp: ENSP00000369082.2:p.Lys1305Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1398G>T
  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.3915G>T
  hgvsp: ENSP00000339620.4:p.Lys1305Asn
  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.3915G>T
  hgvsp: ENSP00000380149.1:p.Lys1305Asn
  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.3915G>T
  hgvsp: ENSP00000309131.5:p.Lys1305Asn
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1879G>T
  hgvsp: ENSP00000430174.1:p.Lys627Asn
  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.4038G>T
  hgvsp: ENSP00000265709.8:p.Lys1346Asn
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys1346Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

8-41548071-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548071
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548071
    reference: chr 8
allele count: 15
allele frequency: 1.241557409614621e-4
allele num: 120816
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.3905T>A
  hgvsp: ENSP00000380147.1:p.Val1302Glu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1869T>A
  hgvsp: ENSP00000430174.1:p.Val624Glu
  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.4028T>A
  hgvsp: ENSP00000265709.8:p.Val1343Glu
  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.3905T>A
  hgvsp: ENSP00000339620.4:p.Val1302Glu
  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.3905T>A
  hgvsp: ENSP00000309131.5:p.Val1302Glu
  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.3905T>A
  hgvsp: ENSP00000289734.7:p.Val1302Glu
  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.3905T>A
  hgvsp: ENSP00000369082.2:p.Val1302Glu
  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.3905T>A
  hgvsp: ENSP00000380149.1:p.Val1302Glu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1388T>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val1343Glu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

8-41548072-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548072
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548072
    reference: chr 8
allele count: 1
allele frequency: 8.278831029058698e-6
allele num: 120790
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.4027G>A
  hgvsp: ENSP00000265709.8:p.Val1343Met
  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.3904G>A
  hgvsp: ENSP00000339620.4:p.Val1302Met
  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.3904G>A
  hgvsp: ENSP00000380147.1:p.Val1302Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1868G>A
  hgvsp: ENSP00000430174.1:p.Val624Met
  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.3904G>A
  hgvsp: ENSP00000289734.7:p.Val1302Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1387G>A
  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.3904G>A
  hgvsp: ENSP00000380149.1:p.Val1302Met
  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.3904G>A
  hgvsp: ENSP00000309131.5:p.Val1302Met
  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.3904G>A
  hgvsp: ENSP00000369082.2:p.Val1302Met
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44196
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val1343Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

8-41548075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548075
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548075
    reference: chr 8
allele count: 8
allele frequency: 6.62471016893011e-5
allele num: 120760
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.3901C>T
  hgvsp: ENST00000379758.2:c.3901C>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.3901C>T
  hgvsp: ENST00000396942.1:c.3901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1865C>T
  hgvsp: ENST00000520299.1:c.1865C>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.3901C>T
  hgvsp: ENST00000396945.1:c.3901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1384C>T
  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.3901C>T
  hgvsp: ENST00000347528.4:c.3901C>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.3901C>T
  hgvsp: ENST00000289734.7:c.3901C>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.3901C>T
  hgvsp: ENST00000352337.4:c.3901C>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.4024C>T
  hgvsp: ENST00000265709.8:c.4024C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu1342Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/8-41548079-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548079
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548079
    reference: chr 8
allele count: 26
allele frequency: 2.15367284052881e-4
allele num: 120724
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.3897G>T
  hgvsp: ENST00000396945.1:c.3897G>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.3897G>T
  hgvsp: ENST00000347528.4:c.3897G>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.3897G>T
  hgvsp: ENST00000396942.1:c.3897G>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.4020G>T
  hgvsp: ENST00000265709.8:c.4020G>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.3897G>T
  hgvsp: ENST00000289734.7:c.3897G>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.3897G>T
  hgvsp: ENST00000379758.2:c.3897G>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.3897G>T
  hgvsp: ENST00000352337.4:c.3897G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1380G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1861G>T
  hgvsp: ENST00000520299.1:c.1861G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44198
  bin: 9.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly1340Gly
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-41548087-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548087
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548087
    reference: chr 8
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1853C>G
  hgvsp: ENSP00000430174.1:p.Leu619Val
  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.3889C>G
  hgvsp: ENSP00000380149.1:p.Leu1297Val
  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.3889C>G
  hgvsp: ENSP00000289734.7:p.Leu1297Val
  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.3889C>G
  hgvsp: ENSP00000380147.1:p.Leu1297Val
  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.3889C>G
  hgvsp: ENSP00000309131.5:p.Leu1297Val
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1372C>G
  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.3889C>G
  hgvsp: ENSP00000339620.4:p.Leu1297Val
  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.3889C>G
  hgvsp: ENSP00000369082.2:p.Leu1297Val
  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.4012C>G
  hgvsp: ENSP00000265709.8:p.Leu1338Val
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu1338Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-41548095-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548095
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548095
    reference: chr 8
allele count: 3
allele frequency: 2.490701381509033e-5
allele num: 120448
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.3881T>A
  hgvsp: ENSP00000309131.5:p.Phe1294Tyr
  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.3881T>A
  hgvsp: ENSP00000369082.2:p.Phe1294Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1845T>A
  hgvsp: ENSP00000430174.1:p.Phe616Tyr
  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.3881T>A
  hgvsp: ENSP00000339620.4:p.Phe1294Tyr
  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.3881T>A
  hgvsp: ENSP00000380149.1:p.Phe1294Tyr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1364T>A
  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.3881T>A
  hgvsp: ENSP00000289734.7:p.Phe1294Tyr
  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.3881T>A
  hgvsp: ENSP00000380147.1:p.Phe1294Tyr
  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.4004T>A
  hgvsp: ENSP00000265709.8:p.Phe1335Tyr
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe1335Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-41548097-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548097
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548097
    reference: chr 8
allele count: 1
allele frequency: 8.306475728477921e-6
allele num: 120388
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.3879G>A
  hgvsp: ENST00000289734.7:c.3879G>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.3879G>A
  hgvsp: ENST00000396945.1:c.3879G>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.3879G>A
  hgvsp: ENST00000379758.2:c.3879G>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.3879G>A
  hgvsp: ENST00000352337.4:c.3879G>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.4002G>A
  hgvsp: ENST00000265709.8:c.4002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1843G>A
  hgvsp: ENST00000520299.1:c.1843G>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.3879G>A
  hgvsp: ENST00000347528.4:c.3879G>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.3879G>A
  hgvsp: ENST00000396942.1:c.3879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1362G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu1334Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

8-41548114-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548114
    reference: chr 8
allele count: 1
allele frequency: 8.34432002136146e-6
allele num: 119842
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.3985T>A
  hgvsp: ENSP00000265709.8:p.Leu1329Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1345T>A
  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.3862T>A
  hgvsp: ENSP00000369082.2:p.Leu1288Met
  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.3862T>A
  hgvsp: ENSP00000380149.1:p.Leu1288Met
  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.3862T>A
  hgvsp: ENSP00000309131.5:p.Leu1288Met
  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.3862T>A
  hgvsp: ENSP00000339620.4:p.Leu1288Met
  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.3862T>A
  hgvsp: ENSP00000289734.7:p.Leu1288Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1826T>A
  hgvsp: ENSP00000430174.1:p.Leu610Met
  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.3862T>A
  hgvsp: ENSP00000380147.1:p.Leu1288Met
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1329Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

8-41548115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548115
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548115
    reference: chr 8
allele count: 2
allele frequency: 1.669058984544514e-5
allele num: 119828
alternate allele: T
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.3984G>A
  hgvsp: ENST00000265709.8:c.3984G>A(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.3861G>A
  hgvsp: ENST00000352337.4:c.3861G>A(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.3861G>A
  hgvsp: ENST00000289734.7:c.3861G>A(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: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1825G>A
  hgvsp: ENST00000520299.1:c.1825G>A(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.3861G>A
  hgvsp: ENST00000347528.4:c.3861G>A(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.3861G>A
  hgvsp: ENST00000396945.1:c.3861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1344G>A
  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.3861G>A
  hgvsp: ENST00000396942.1:c.3861G>A(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: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.3861G>A
  hgvsp: ENST00000379758.2:c.3861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
hgvs: c.3984G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

8-41548117-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548117
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548117
    reference: chr 8
allele count: 1
allele frequency: 8.348917980229763e-6
allele num: 119776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000339620
  ensembl transcript: ENST00000347528
  gene symbol: ANK1
  hgvsc: ENST00000347528.4:c.3859G>C
  hgvsp: ENSP00000339620.4:p.Val1287Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.3859G>C
  hgvsp: ENSP00000380149.1:p.Val1287Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.3859G>C
  hgvsp: ENSP00000369082.2:p.Val1287Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823G>C
  hgvsp: ENSP00000430174.1:p.Val609Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.3982G>C
  hgvsp: ENSP00000265709.8:p.Val1328Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3859G>C
  hgvsp: ENSP00000380147.1:p.Val1287Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342G>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.3859G>C
  hgvsp: ENSP00000309131.5:p.Val1287Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.3859G>C
  hgvsp: ENSP00000289734.7:p.Val1287Leu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1328Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

8-41548126-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548126
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548126
    reference: chr 8
allele count: 1
allele frequency: 8.366100560528738e-6
allele num: 119530
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-9C>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.3859-9C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-9C>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.3859-9C>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.3859-9C>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.3982-9C>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.3859-9C>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.3859-9C>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.3859-9C>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

8-41548133-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548133
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548133
    reference: chr 8
allele count: 1
allele frequency: 8.381386616601851e-6
allele num: 119312
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.3859-16T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-16T>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.3982-16T>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.3859-16T>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.3859-16T>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-16T>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.3859-16T>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.3859-16T>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.3859-16T>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44184
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

8-41548147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548147
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548147
    reference: chr 8
allele count: 1
allele frequency: 8.406469619018796e-6
allele num: 118956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-30C>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.3859-30C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-30C>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.3859-30C>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.3859-30C>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.3982-30C>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.3859-30C>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.3859-30C>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.3859-30C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-41548153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548153
    reference: chr 8
allele count: 1
allele frequency: 8.418075291265404e-6
allele num: 118792
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.3982-36C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-36C>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.3859-36C>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.3859-36C>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.3859-36C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-36C>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.3859-36C>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.3859-36C>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.3859-36C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

8-41548153-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548153
    reference: chr 8
allele count: 467
allele frequency: 3.931241161020944e-3
allele num: 118792
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.3982-36C>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.3859-36C>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.3859-36C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-36C>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.3859-36C>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.3859-36C>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.3859-36C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-36C>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.3859-36C>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 9.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 8.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44263
  bin: 9.75e1
  variant carriers: 461
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 5
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

8-41548160-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548160
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548160
    reference: chr 8
allele count: 1
allele frequency: 8.434263351438885e-6
allele num: 118564
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.3982-43C>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.3859-43C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-43C>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.3859-43C>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.3859-43C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-43C>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.3859-43C>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.3859-43C>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.3859-43C>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-41548161-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41548161
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41548161
    reference: chr 8
allele count: 1
allele frequency: 8.435970980259829e-6
allele num: 118540
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.3982-44C>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.3859-44C>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.3859-44C>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.3859-44C>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.3859-44C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1823-44C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1342-44C>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.3859-44C>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.3859-44C>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

8-41550118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550118
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550118
    reference: chr 8
allele count: 10
allele frequency: 8.294625082946251e-5
allele num: 120560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3858+48G>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.3858+48G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+48G>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.3981+48G>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.3858+48G>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.3858+48G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+48G>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.3858+48G>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.3858+48G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-41550119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550119
    reference: chr 8
allele count: 6
allele frequency: 4.971908715755978e-5
allele num: 120678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+47C>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.3858+47C>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.3858+47C>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.3858+47C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+47C>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.3858+47C>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.3858+47C>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.3858+47C>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.3981+47C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4040
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-41550119-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550119
    reference: chr 8
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.3858+47C>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.3858+47C>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.3858+47C>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.3981+47C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+47C>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.3858+47C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+47C>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.3858+47C>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.3858+47C>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6975
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

8-41550126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550126
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550126
    reference: chr 8
allele count: 3
allele frequency: 2.48562480322137e-5
allele num: 120694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+40G>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.3858+40G>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.3858+40G>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.3858+40G>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.3858+40G>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.3858+40G>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.3858+40G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+40G>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.3981+40G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

8-41550128-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550128
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550128
    reference: chr 8
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
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.3858+38C>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.3858+38C>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.3858+38C>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.3858+38C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+38C>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.3981+38C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+38C>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.3858+38C>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.3858+38C>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7558
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2037
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

8-41550132-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550132
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550132
    reference: chr 8
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
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.3858+34C>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.3858+34C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+34C>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.3981+34C>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.3858+34C>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.3858+34C>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.3858+34C>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+34C>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.3858+34C>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-41550138-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550138
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550138
    reference: chr 8
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.3858+28C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+28C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+28C>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.3858+28C>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.3858+28C>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.3858+28C>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.3858+28C>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.3858+28C>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.3981+28C>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-41550142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550142
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550142
    reference: chr 8
allele count: 2
allele frequency: 1.66281447978849e-5
allele num: 120278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.3858+24G>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.3981+24G>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.3858+24G>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.3858+24G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+24G>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.3858+24G>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.3858+24G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+24G>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.3858+24G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33060
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7775
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

8-41550143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550143
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550143
    reference: chr 8
allele count: 1
allele frequency: 8.30937463646486e-6
allele num: 120346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3858+23C>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.3981+23C>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.3858+23C>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.3858+23C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+23C>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.3858+23C>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.3858+23C>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.3858+23C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+23C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
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: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

8-41550143-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550143
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550143
    reference: chr 8
allele count: 1
allele frequency: 8.30937463646486e-6
allele num: 120346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3858+23C>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.3858+23C>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.3858+23C>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.3858+23C>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.3858+23C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+23C>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+23C>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.3981+23C>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.3858+23C>G
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-41550147-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550147
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550147
    reference: chr 8
allele count: 1
allele frequency: 8.278831029058698e-6
allele num: 120790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.3858+19G>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.3981+19G>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.3858+19G>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.3858+19G>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.3858+19G>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+19G>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.3858+19G>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.3858+19G>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+19G>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

8-41550152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550152
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550152
    reference: chr 8
allele count: 1
allele frequency: 8.276227364518158e-6
allele num: 120828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+14G>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.3858+14G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+14G>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.3858+14G>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.3858+14G>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.3981+14G>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.3858+14G>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.3858+14G>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.3858+14G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8181
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-41550153-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550153
    reference: chr 8
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000265709
  ensembl transcript: ENST00000265709
  gene symbol: ANK1
  hgvsc: ENST00000265709.8:c.3981+13G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+13G>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.3858+13G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+13G>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.3858+13G>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.3858+13G>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.3858+13G>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.3858+13G>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.3858+13G>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33194
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/8-41550157-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550157
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550157
    reference: chr 8
allele count: 2
allele frequency: 1.654259718775848e-5
allele num: 120900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+9G>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.3858+9G>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.3858+9G>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.3858+9G>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.3981+9G>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+9G>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.3858+9G>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.3858+9G>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.3858+9G>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2021
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

8-41550160-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550160
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550160
    reference: chr 8
allele count: 4
allele frequency: 3.307972213033411e-5
allele num: 120920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1341+6A>C
  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.3858+6A>C
  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.3858+6A>C
  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.3981+6A>C
  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.3858+6A>C
  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.3858+6A>C
  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.3858+6A>C
  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.3858+6A>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1822+6A>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
hgvs: c.3981+6A>C
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

8-41550183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550183
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550183
    reference: chr 8
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.3841C>T
  hgvsp: ENSP00000380149.1:p.Arg1281Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.710C>T
  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.3841C>T
  hgvsp: ENSP00000369082.2:p.Arg1281Trp
  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.3964C>T
  hgvsp: ENSP00000265709.8:p.Arg1322Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1805C>T
  hgvsp: ENSP00000430174.1:p.Arg603Trp
  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.3841C>T
  hgvsp: ENSP00000289734.7:p.Arg1281Trp
  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.3841C>T
  hgvsp: ENSP00000339620.4:p.Arg1281Trp
  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.3841C>T
  hgvsp: ENSP00000380147.1:p.Arg1281Trp
  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.3841C>T
  hgvsp: ENSP00000309131.5:p.Arg1281Trp
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1324C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1322Trp
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-41550195-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550195
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550195
    reference: chr 8
allele count: 11
allele frequency: 9.072314594879915e-5
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.3829G>C
  hgvsp: ENSP00000380149.1:p.Val1277Leu
  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.3829G>C
  hgvsp: ENSP00000380147.1:p.Val1277Leu
  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.3829G>C
  hgvsp: ENSP00000289734.7:p.Val1277Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.698G>C
  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.3829G>C
  hgvsp: ENSP00000339620.4:p.Val1277Leu
  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.3829G>C
  hgvsp: ENSP00000309131.5:p.Val1277Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1312G>C
  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.3829G>C
  hgvsp: ENSP00000369082.2:p.Val1277Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1793G>C
  hgvsp: ENSP00000430174.1:p.Val599Leu
  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.3952G>C
  hgvsp: ENSP00000265709.8:p.Val1318Leu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val1318Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-41550195-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550195
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550195
    reference: chr 8
allele count: 100
allele frequency: 8.247558722618105e-4
allele num: 121248
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.3829G>A
  hgvsp: ENSP00000369082.2:p.Val1277Met
  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.3829G>A
  hgvsp: ENSP00000380149.1:p.Val1277Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.698G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1312G>A
  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.3952G>A
  hgvsp: ENSP00000265709.8:p.Val1318Met
  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.3829G>A
  hgvsp: ENSP00000380147.1:p.Val1277Met
  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.3829G>A
  hgvsp: ENSP00000289734.7:p.Val1277Met
  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.3829G>A
  hgvsp: ENSP00000339620.4:p.Val1277Met
  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.3829G>A
  hgvsp: ENSP00000309131.5:p.Val1277Met
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1793G>A
  hgvsp: ENSP00000430174.1:p.Val599Met
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7977
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8618
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val1318Met
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

8-41550196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550196
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550196
    reference: chr 8
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
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.3828C>T
  hgvsp: ENST00000379758.2:c.3828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1792C>T
  hgvsp: ENST00000520299.1:c.1792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.697C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1311C>T
  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.3828C>T
  hgvsp: ENST00000347528.4:c.3828C>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.3828C>T
  hgvsp: ENST00000396945.1:c.3828C>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.3951C>T
  hgvsp: ENST00000265709.8:c.3951C>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.3828C>T
  hgvsp: ENST00000289734.7:c.3828C>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.3828C>T
  hgvsp: ENST00000396942.1:c.3828C>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.3828C>T
  hgvsp: ENST00000352337.4:c.3828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe1317Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-41550202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550202
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550202
    reference: chr 8
allele count: 2
allele frequency: 1.648804616652927e-5
allele num: 121300
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.3945G>A
  hgvsp: ENST00000265709.8:c.3945G>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.3822G>A
  hgvsp: ENST00000347528.4:c.3822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.691G>A
  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.3822G>A
  hgvsp: ENST00000289734.7:c.3822G>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.3822G>A
  hgvsp: ENST00000396942.1:c.3822G>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.3822G>A
  hgvsp: ENST00000352337.4:c.3822G>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.3822G>A
  hgvsp: ENST00000396945.1:c.3822G>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.3822G>A
  hgvsp: ENST00000379758.2:c.3822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1786G>A
  hgvsp: ENST00000520299.1:c.1786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1305G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4253
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu1315Glu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-41550210-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550210
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550210
    reference: chr 8
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
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.3814C>G
  hgvsp: ENSP00000369082.2:p.Gln1272Glu
  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.3814C>G
  hgvsp: ENSP00000380149.1:p.Gln1272Glu
  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.3814C>G
  hgvsp: ENSP00000309131.5:p.Gln1272Glu
  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.3814C>G
  hgvsp: ENSP00000289734.7:p.Gln1272Glu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1778C>G
  hgvsp: ENSP00000430174.1:p.Gln594Glu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.683C>G
  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.3814C>G
  hgvsp: ENSP00000339620.4:p.Gln1272Glu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1297C>G
  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.3937C>G
  hgvsp: ENSP00000265709.8:p.Gln1313Glu
  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.3814C>G
  hgvsp: ENSP00000380147.1:p.Gln1272Glu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln1313Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

8-41550211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550211
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550211
    reference: chr 8
allele count: 419
allele frequency: 3.453790101882687e-3
allele num: 121316
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.3813G>A
  hgvsp: ENST00000396942.1:c.3813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1777G>A
  hgvsp: ENST00000520299.1:c.1777G>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.3813G>A
  hgvsp: ENST00000352337.4:c.3813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.682G>A
  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.3813G>A
  hgvsp: ENST00000289734.7:c.3813G>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.3936G>A
  hgvsp: ENST00000265709.8:c.3936G>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.3813G>A
  hgvsp: ENST00000396945.1:c.3813G>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.3813G>A
  hgvsp: ENST00000347528.4:c.3813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1296G>A
  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.3813G>A
  hgvsp: ENST00000379758.2:c.3813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 9.75e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu1312Glu
num of homozygotes: 6
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-41550216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550216
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550216
    reference: chr 8
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
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.3808C>T
  hgvsp: ENST00000396945.1:c.3808C>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.3931C>T
  hgvsp: ENST00000265709.8:c.3931C>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.3808C>T
  hgvsp: ENST00000379758.2:c.3808C>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.3808C>T
  hgvsp: ENST00000347528.4:c.3808C>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.3808C>T
  hgvsp: ENST00000289734.7:c.3808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1772C>T
  hgvsp: ENST00000520299.1:c.1772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.677C>T
  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.3808C>T
  hgvsp: ENST00000396942.1:c.3808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1291C>T
  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.3808C>T
  hgvsp: ENST00000352337.4:c.3808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8687
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33035
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu1311Leu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-41550253-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550253
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550253
    reference: chr 8
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
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.3771C>G
  hgvsp: ENST00000396942.1:c.3771C>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.3771C>G
  hgvsp: ENST00000352337.4:c.3771C>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.3771C>G
  hgvsp: ENST00000347528.4:c.3771C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1254C>G
  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.3771C>G
  hgvsp: ENST00000379758.2:c.3771C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1735C>G
  hgvsp: ENST00000520299.1:c.1735C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.640C>G
  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.3771C>G
  hgvsp: ENST00000396945.1:c.3771C>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.3771C>G
  hgvsp: ENST00000289734.7:c.3771C>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.3894C>G
  hgvsp: ENST00000265709.8:c.3894C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1298Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-41550254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550254
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550254
    reference: chr 8
allele count: 6
allele frequency: 4.944212798918866e-5
allele num: 121354
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.3893G>A
  hgvsp: ENSP00000265709.8:p.Arg1298His
  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.3770G>A
  hgvsp: ENSP00000309131.5:p.Arg1257His
  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.3770G>A
  hgvsp: ENSP00000380147.1:p.Arg1257His
  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.3770G>A
  hgvsp: ENSP00000380149.1:p.Arg1257His
  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.3770G>A
  hgvsp: ENSP00000289734.7:p.Arg1257His
  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.3770G>A
  hgvsp: ENSP00000369082.2:p.Arg1257His
  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.3770G>A
  hgvsp: ENSP00000339620.4:p.Arg1257His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1253G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1734G>A
  hgvsp: ENSP00000430174.1:p.Arg579His
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.639G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4268
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg1298His
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-41550255-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550255
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550255
    reference: chr 8
allele count: 4
allele frequency: 3.296087544085171e-5
allele num: 121356
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.3769C>T
  hgvsp: ENSP00000289734.7:p.Arg1257Cys
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.638C>T
  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.3892C>T
  hgvsp: ENSP00000265709.8:p.Arg1298Cys
  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.3769C>T
  hgvsp: ENSP00000380149.1:p.Arg1257Cys
  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.3769C>T
  hgvsp: ENSP00000339620.4:p.Arg1257Cys
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1252C>T
  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.3769C>T
  hgvsp: ENSP00000380147.1:p.Arg1257Cys
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1733C>T
  hgvsp: ENSP00000430174.1:p.Arg579Cys
  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.3769C>T
  hgvsp: ENSP00000309131.5:p.Arg1257Cys
  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.3769C>T
  hgvsp: ENSP00000369082.2:p.Arg1257Cys
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 33034
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1298Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-41550255-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550255
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550255
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
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.3769C>A
  hgvsp: ENSP00000289734.7:p.Arg1257Ser
  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.3769C>A
  hgvsp: ENSP00000380147.1:p.Arg1257Ser
  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.3769C>A
  hgvsp: ENSP00000369082.2:p.Arg1257Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1733C>A
  hgvsp: ENSP00000430174.1:p.Arg579Ser
  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.3769C>A
  hgvsp: ENSP00000380149.1:p.Arg1257Ser
  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.3892C>A
  hgvsp: ENSP00000265709.8:p.Arg1298Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.638C>A
  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.3769C>A
  hgvsp: ENSP00000309131.5:p.Arg1257Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1252C>A
  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.3769C>A
  hgvsp: ENSP00000339620.4:p.Arg1257Ser
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg1298Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

8-41550261-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550261
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550261
    reference: chr 8
allele count: 31
allele frequency: 2.55594215325759e-4
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000369082
  ensembl transcript: ENST00000379758
  gene symbol: ANK1
  hgvsc: ENST00000379758.2:c.3763C>T
  hgvsp: ENSP00000369082.2:p.Arg1255Cys
  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.3763C>T
  hgvsp: ENSP00000380149.1:p.Arg1255Cys
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1246C>T
  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.3763C>T
  hgvsp: ENSP00000339620.4:p.Arg1255Cys
  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.3763C>T
  hgvsp: ENSP00000309131.5:p.Arg1255Cys
  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.3763C>T
  hgvsp: ENSP00000380147.1:p.Arg1255Cys
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1727C>T
  hgvsp: ENSP00000430174.1:p.Arg577Cys
  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.3886C>T
  hgvsp: ENSP00000265709.8:p.Arg1296Cys
  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.3763C>T
  hgvsp: ENSP00000289734.7:p.Arg1255Cys
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.632C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg1296Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

8-41550268-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550268
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550268
    reference: chr 8
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1239A>G
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1720A>G
  hgvsp: ENST00000520299.1:c.1720A>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.3756A>G
  hgvsp: ENST00000347528.4:c.3756A>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.3756A>G
  hgvsp: ENST00000289734.7:c.3756A>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.3756A>G
  hgvsp: ENST00000379758.2:c.3756A>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.3756A>G
  hgvsp: ENST00000396945.1:c.3756A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.625A>G
  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.3756A>G
  hgvsp: ENST00000352337.4:c.3756A>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.3879A>G
  hgvsp: ENST00000265709.8:c.3879A>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.3756A>G
  hgvsp: ENST00000396942.1:c.3756A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1293Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/8-41550269-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550269
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550269
    reference: chr 8
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1238G>T
  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.3755G>T
  hgvsp: ENSP00000339620.4:p.Arg1252Leu
  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.3755G>T
  hgvsp: ENSP00000369082.2:p.Arg1252Leu
  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.3755G>T
  hgvsp: ENSP00000289734.7:p.Arg1252Leu
  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.3878G>T
  hgvsp: ENSP00000265709.8:p.Arg1293Leu
  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.3755G>T
  hgvsp: ENSP00000380149.1:p.Arg1252Leu
  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.3755G>T
  hgvsp: ENSP00000380147.1:p.Arg1252Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1719G>T
  hgvsp: ENSP00000430174.1:p.Arg574Leu
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.624G>T
  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.3755G>T
  hgvsp: ENSP00000309131.5:p.Arg1252Leu
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8409
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg1293Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-41550281-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550281
    reference: chr 8
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3743T>C
  hgvsp: ENSP00000380147.1:p.Met1248Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1707T>C
  hgvsp: ENSP00000430174.1:p.Met570Thr
  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.3743T>C
  hgvsp: ENSP00000339620.4:p.Met1248Thr
  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.3743T>C
  hgvsp: ENSP00000289734.7:p.Met1248Thr
  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.3743T>C
  hgvsp: ENSP00000369082.2:p.Met1248Thr
  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.3743T>C
  hgvsp: ENSP00000380149.1:p.Met1248Thr
  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.3866T>C
  hgvsp: ENSP00000265709.8:p.Met1289Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.612T>C
  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.3743T>C
  hgvsp: ENSP00000309131.5:p.Met1248Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1226T>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4313
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met1289Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

8-41550295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550295
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550295
    reference: chr 8
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1212C>T
  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.3729C>T
  hgvsp: ENST00000289734.7:c.3729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1693C>T
  hgvsp: ENST00000520299.1:c.1693C>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.3729C>T
  hgvsp: ENST00000396945.1:c.3729C>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.3729C>T
  hgvsp: ENST00000352337.4:c.3729C>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.3729C>T
  hgvsp: ENST00000396942.1:c.3729C>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.3729C>T
  hgvsp: ENST00000379758.2:c.3729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.598C>T
  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.3729C>T
  hgvsp: ENST00000347528.4:c.3729C>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.3852C>T
  hgvsp: ENST00000265709.8:c.3852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val1284Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

8-41550296-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550296
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550296
    reference: chr 8
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.3728T>C
  hgvsp: ENSP00000380149.1:p.Val1243Ala
  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.3728T>C
  hgvsp: ENSP00000289734.7:p.Val1243Ala
  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.3728T>C
  hgvsp: ENSP00000369082.2:p.Val1243Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.597T>C
  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.3728T>C
  hgvsp: ENSP00000339620.4:p.Val1243Ala
  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.3728T>C
  hgvsp: ENSP00000380147.1:p.Val1243Ala
  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.3728T>C
  hgvsp: ENSP00000309131.5:p.Val1243Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1211T>C
  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.3851T>C
  hgvsp: ENSP00000265709.8:p.Val1284Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1692T>C
  hgvsp: ENSP00000430174.1:p.Val565Ala
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val1284Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-41550297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550297
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550297
    reference: chr 8
allele count: 8
allele frequency: 6.599135513247765e-5
allele num: 121228
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.3727G>A
  hgvsp: ENSP00000380147.1:p.Val1243Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1691G>A
  hgvsp: ENSP00000430174.1:p.Val565Ile
  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.3727G>A
  hgvsp: ENSP00000309131.5:p.Val1243Ile
  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.3727G>A
  hgvsp: ENSP00000380149.1:p.Val1243Ile
  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.3727G>A
  hgvsp: ENSP00000289734.7:p.Val1243Ile
  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.3727G>A
  hgvsp: ENSP00000369082.2:p.Val1243Ile
  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.3850G>A
  hgvsp: ENSP00000265709.8:p.Val1284Ile
  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.3727G>A
  hgvsp: ENSP00000339620.4:p.Val1243Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1210G>A
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.596G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val1284Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

8-41550298-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550298
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550298
    reference: chr 8
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1209C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1690C>T
  hgvsp: ENST00000520299.1:c.1690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.595C>T
  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.3726C>T
  hgvsp: ENST00000396942.1:c.3726C>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.3726C>T
  hgvsp: ENST00000379758.2:c.3726C>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.3726C>T
  hgvsp: ENST00000289734.7:c.3726C>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.3726C>T
  hgvsp: ENST00000347528.4:c.3726C>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.3726C>T
  hgvsp: ENST00000396945.1:c.3726C>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.3849C>T
  hgvsp: ENST00000265709.8:c.3849C>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.3726C>T
  hgvsp: ENST00000352337.4:c.3726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33032
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Phe1283Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

8-41550315-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550315
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550315
    reference: chr 8
allele count: 2
allele frequency: 1.65188231990353e-5
allele num: 121074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1192C>A
  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.3709C>A
  hgvsp: ENSP00000380147.1:p.Pro1237Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1673C>A
  hgvsp: ENSP00000430174.1:p.Pro559Thr
  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.3709C>A
  hgvsp: ENSP00000309131.5:p.Pro1237Thr
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.578C>A
  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.3709C>A
  hgvsp: ENSP00000369082.2:p.Pro1237Thr
  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.3709C>A
  hgvsp: ENSP00000380149.1:p.Pro1237Thr
  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.3709C>A
  hgvsp: ENSP00000289734.7:p.Pro1237Thr
  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.3709C>A
  hgvsp: ENSP00000339620.4:p.Pro1237Thr
  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.3832C>A
  hgvsp: ENSP00000265709.8:p.Pro1278Thr
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1278Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-41550339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550339
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550339
    reference: chr 8
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000289734
  ensembl transcript: ENST00000289734
  gene symbol: ANK1
  hgvsc: ENST00000289734.7:c.3685C>T
  hgvsp: ENST00000289734.7:c.3685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.554C>T
  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.3808C>T
  hgvsp: ENST00000265709.8:c.3808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1649C>T
  hgvsp: ENST00000520299.1:c.1649C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1168C>T
  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.3685C>T
  hgvsp: ENST00000396945.1:c.3685C>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.3685C>T
  hgvsp: ENST00000347528.4:c.3685C>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.3685C>T
  hgvsp: ENST00000379758.2:c.3685C>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.3685C>T
  hgvsp: ENST00000396942.1:c.3685C>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.3685C>T
  hgvsp: ENST00000352337.4:c.3685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu1270Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

8-41550343-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550343
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550343
    reference: chr 8
allele count: 2
allele frequency: 1.654779831543413e-5
allele num: 120862
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.3681C>G
  hgvsp: ENST00000396945.1:c.3681C>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.3681C>G
  hgvsp: ENST00000379758.2:c.3681C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1645C>G
  hgvsp: ENST00000520299.1:c.1645C>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.3804C>G
  hgvsp: ENST00000265709.8:c.3804C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.550C>G
  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.3681C>G
  hgvsp: ENST00000347528.4:c.3681C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1164C>G
  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.3681C>G
  hgvsp: ENST00000352337.4:c.3681C>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.3681C>G
  hgvsp: ENST00000289734.7:c.3681C>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.3681C>G
  hgvsp: ENST00000396942.1:c.3681C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr1268Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-41550344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550344
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550344
    reference: chr 8
allele count: 2
allele frequency: 1.655053706492776e-5
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380149
  ensembl transcript: ENST00000396945
  gene symbol: ANK1
  hgvsc: ENST00000396945.1:c.3680C>T
  hgvsp: ENSP00000380149.1:p.Thr1227Ile
  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.3803C>T
  hgvsp: ENSP00000265709.8:p.Thr1268Ile
  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.3680C>T
  hgvsp: ENSP00000369082.2:p.Thr1227Ile
  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.3680C>T
  hgvsp: ENSP00000289734.7:p.Thr1227Ile
  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.3680C>T
  hgvsp: ENSP00000309131.5:p.Thr1227Ile
  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.3680C>T
  hgvsp: ENSP00000380147.1:p.Thr1227Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.549C>T
  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.3680C>T
  hgvsp: ENSP00000339620.4:p.Thr1227Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1644C>T
  hgvsp: ENSP00000430174.1:p.Thr549Ile
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1163C>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr1268Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

8-41550345-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550345
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550345
    reference: chr 8
allele count: 4
allele frequency: 3.309943068979214e-5
allele num: 120848
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.3679A>T
  hgvsp: ENSP00000380147.1:p.Thr1227Ser
  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.3679A>T
  hgvsp: ENSP00000339620.4:p.Thr1227Ser
  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.3679A>T
  hgvsp: ENSP00000309131.5:p.Thr1227Ser
  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.3679A>T
  hgvsp: ENSP00000289734.7:p.Thr1227Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1643A>T
  hgvsp: ENSP00000430174.1:p.Thr549Ser
  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.3679A>T
  hgvsp: ENSP00000369082.2:p.Thr1227Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1162A>T
  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.3679A>T
  hgvsp: ENSP00000380149.1:p.Thr1227Ser
  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.3802A>T
  hgvsp: ENSP00000265709.8:p.Thr1268Ser
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.548A>T
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr1268Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-41550352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550352
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550352
    reference: chr 8
allele count: 2
allele frequency: 1.655930715858849e-5
allele num: 120778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1636C>T
  hgvsp: ENST00000520299.1:c.1636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.541C>T
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1155C>T
  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.3672C>T
  hgvsp: ENST00000379758.2:c.3672C>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.3672C>T
  hgvsp: ENST00000347528.4:c.3672C>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.3672C>T
  hgvsp: ENST00000289734.7:c.3672C>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.3672C>T
  hgvsp: ENST00000396942.1:c.3672C>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.3672C>T
  hgvsp: ENST00000396945.1:c.3672C>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.3672C>T
  hgvsp: ENST00000352337.4:c.3672C>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.3795C>T
  hgvsp: ENST00000265709.8:c.3795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7640
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn1265Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

8-41550356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550356
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550356
    reference: chr 8
allele count: 122
allele frequency: 1.010569563632749e-3
allele num: 120724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1151T>C
  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.3668T>C
  hgvsp: ENSP00000380149.1:p.Val1223Ala
  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.3668T>C
  hgvsp: ENSP00000309131.5:p.Val1223Ala
  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.3668T>C
  hgvsp: ENSP00000289734.7:p.Val1223Ala
  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.3668T>C
  hgvsp: ENSP00000380147.1:p.Val1223Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.537T>C
  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.3668T>C
  hgvsp: ENSP00000339620.4:p.Val1223Ala
  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.3791T>C
  hgvsp: ENSP00000265709.8:p.Val1264Ala
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1632T>C
  hgvsp: ENSP00000430174.1:p.Val545Ala
  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.3668T>C
  hgvsp: ENSP00000369082.2:p.Val1223Ala
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1264Ala
num of homozygotes: 1
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-41550358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550358
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550358
    reference: chr 8
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000380147
  ensembl transcript: ENST00000396942
  gene symbol: ANK1
  hgvsc: ENST00000396942.1:c.3666T>C
  hgvsp: ENST00000396942.1:c.3666T>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.3666T>C
  hgvsp: ENST00000352337.4:c.3666T>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.3666T>C
  hgvsp: ENST00000379758.2:c.3666T>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.3789T>C
  hgvsp: ENST00000265709.8:c.3789T>C(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.3666T>C
  hgvsp: ENST00000347528.4:c.3666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1149T>C
  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.3666T>C
  hgvsp: ENST00000396945.1:c.3666T>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.3666T>C
  hgvsp: ENST00000289734.7:c.3666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.535T>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1630T>C
  hgvsp: ENST00000520299.1:c.1630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala1263Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-41550361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550361
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550361
    reference: chr 8
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
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.3786G>A
  hgvsp: ENST00000265709.8:c.3786G>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.3663G>A
  hgvsp: ENST00000347528.4:c.3663G>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.3663G>A
  hgvsp: ENST00000352337.4:c.3663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1627G>A
  hgvsp: ENST00000520299.1:c.1627G>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.3663G>A
  hgvsp: ENST00000289734.7:c.3663G>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.3663G>A
  hgvsp: ENST00000396945.1:c.3663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.532G>A
  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.3663G>A
  hgvsp: ENST00000379758.2:c.3663G>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.3663G>A
  hgvsp: ENST00000396942.1:c.3663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1146G>A
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu1262Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

8-41550366-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550366
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550366
    reference: chr 8
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
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.3658G>C
  hgvsp: ENSP00000369082.2:p.Ala1220Pro
  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.3658G>C
  hgvsp: ENSP00000380147.1:p.Ala1220Pro
  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.3658G>C
  hgvsp: ENSP00000380149.1:p.Ala1220Pro
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1141G>C
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.527G>C
  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.3658G>C
  hgvsp: ENSP00000339620.4:p.Ala1220Pro
  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.3658G>C
  hgvsp: ENSP00000289734.7:p.Ala1220Pro
  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.3781G>C
  hgvsp: ENSP00000265709.8:p.Ala1261Pro
  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.3658G>C
  hgvsp: ENSP00000309131.5:p.Ala1220Pro
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1622G>C
  hgvsp: ENSP00000430174.1:p.Ala542Pro
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7743
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala1261Pro
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-41550370-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41550370
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 41550370
    reference: chr 8
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000309131
  ensembl transcript: ENST00000352337
  gene symbol: ANK1
  hgvsc: ENST00000352337.4:c.3654G>C
  hgvsp: ENST00000352337.4:c.3654G>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.3777G>C
  hgvsp: ENST00000265709.8:c.3777G>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.3654G>C
  hgvsp: ENST00000396945.1:c.3654G>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.3654G>C
  hgvsp: ENST00000289734.7:c.3654G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029534
  ensembl protein: ENSP00000430174
  ensembl transcript: ENST00000520299
  gene symbol: ANK1
  hgvsc: ENST00000520299.1:c.1618G>C
  hgvsp: ENST00000520299.1:c.1618G>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.3654G>C
  hgvsp: ENST00000396942.1:c.3654G>C(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.3654G>C
  hgvsp: ENST00000347528.4:c.3654G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524227
  gene symbol: ANK1
  hgvsc: ENST00000524227.1:n.1137G>C
  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.3654G>C
  hgvsp: ENST00000379758.2:c.3654G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/492
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029534
  ensembl transcript: ENST00000524069
  gene symbol: ANK1
  hgvsc: ENST00000524069.1:n.523G>C
  variant of: http://identifiers.org/hgnc/492
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg1259Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

8-41550371-C-T
type: Variant
allele count: 8
allele frequency: 6.643745743850382e-5
allele num: 120414
alternate allele: T
canonical: true
consequence: missense
filter: PASS
hgvs: p.Arg1259Gln
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2492
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44244
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5011
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 5
allele frequency: 5.80046403712297e-4
allele num: 8620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

FS
type: SiteQuality
SIO_000300: 2.945e0

DP
type: SiteQuality
SIO_000300: 3.430195e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.519e1

GenotypeQuality
all individuals: 1966
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1416
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2136
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1857
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44248
bin: 9.75e1
variant carriers: 23

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.931207762952695e-4
allele num: 11542
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.801477211313277e-4
allele num: 66612
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

DP
type: SiteQuality
SIO_000300: 3.43049e6

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.18e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.35e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2477
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44204
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
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: 11542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

DP
type: SiteQuality
SIO_000300: 3.427541e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44197
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.513825438807405e-5
allele num: 66544
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.424507e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.79e-2

FS
type: SiteQuality
SIO_000300: 1.123e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44198
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 2119
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4914
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005530175522962e-5
allele num: 66544
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.28e1

DP
type: SiteQuality
SIO_000300: 3.424368e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5083
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44199
bin: 9.75e1
variant carriers: 1

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: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.785e0

FS
type: SiteQuality
SIO_000300: 7.836e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.935e1

DP
type: SiteQuality
SIO_000300: 3.42369e6

VQSLOD
type: SiteQuality
SIO_000300: -2.239e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

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

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

GenotypeQuality
all individuals: 44199
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.020469596628537e-5
allele num: 66440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.66616176916086e-3
allele num: 6602
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.478e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.068e0

DP
type: SiteQuality
SIO_000300: 3.42283e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.194e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1176
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 435
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505343971097396e-5
allele num: 66430
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.421526e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

QD
type: SiteQuality
SIO_000300: 1.094e1

FS
type: SiteQuality
SIO_000300: 8.747999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.672e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.255e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

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

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44196
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 451
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4943
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66408
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 8
allele frequency: 4.853779881082393e-4
allele num: 16482
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

DP
type: SiteQuality
SIO_000300: 3.421539e6

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.274e1

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

GenotypeQuality
all individuals: 1870
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4916
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1805
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1403
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 26
allele frequency: 3.03951367781155e-3
allele num: 8554
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: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66386
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.887e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.081e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

DP
type: SiteQuality
SIO_000300: 3.421833e6

GenotypeQuality
all individuals: 1402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1862
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4842
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Finnish)
type: Population
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: 10250
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507749834147518e-5
allele num: 66324
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.111e1

DP
type: SiteQuality
SIO_000300: 3.418277e6

VQSLOD
type: SiteQuality
SIO_000300: 4.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.804e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

GenotypeQuality
all individuals: 698
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44191
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 7.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.530763886791313e-5
allele num: 66214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

DP
type: SiteQuality
SIO_000300: 3.415514e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.369e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.333e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.091e1

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

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

GenotypeQuality
all individuals: 44191
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1815
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Finnish)
type: Population
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: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66172
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

DP
type: SiteQuality
SIO_000300: 3.413745e6

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 9.68e0

FS
type: SiteQuality
SIO_000300: 7.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.048e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.695e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

GenotypeQuality
all individuals: 2478
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44187
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65828
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.904912836767037e-5
allele num: 10096
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.191e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.163e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

DP
type: SiteQuality
SIO_000300: 3.398665e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeQuality
all individuals: 2100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3683
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44186
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038867110341265e-5
allele num: 65814
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.398009e6

QD
type: SiteQuality
SIO_000300: 1.157e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.522e0

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

GenotypeQuality
all individuals: 3657
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 266
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44186
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 129
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1751
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65776
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

QD
type: SiteQuality
SIO_000300: 1.474e1

DP
type: SiteQuality
SIO_000300: 3.396637e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 1739
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2092
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524204365321302e-5
allele num: 65608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 3.39064e6

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

GenotypeQuality
all individuals: 2911
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527743827914935e-5
allele num: 65456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

FS
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 3.384532e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44184
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533789380042332e-5
allele num: 65198
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.138e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 3.376422e6

MQ
type: SiteQuality
SIO_000300: 5.848e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.057e0

VQSLOD
type: SiteQuality
SIO_000300: -1.865e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.038e0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1368
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2451
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65090
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
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: 1
allele frequency: 1.009489198465576e-4
allele num: 9906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.75e-1

DP
type: SiteQuality
SIO_000300: 3.376927e6

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

QD
type: SiteQuality
SIO_000300: 1.457e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.15e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 2455
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 2.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 170
allele frequency: 2.611768320786603e-3
allele num: 65090
num of homozygotes: 2

African
type: Population
allele count: 5
allele frequency: 5.047445992327882e-4
allele num: 9906
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

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

Latino
type: Population
allele count: 21
allele frequency: 1.83182135380321e-3
allele num: 11464
num of homozygotes: 0

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

South Asian
type: Population
allele count: 270
allele frequency: 1.641137855579869e-2
allele num: 16452
num of homozygotes: 3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 3.376927e6

FS
type: SiteQuality
SIO_000300: 7.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

QD
type: SiteQuality
SIO_000300: 1.457e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.15e-2

GenotypeQuality
all individuals: 466
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 333
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44165
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1389
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540167570231641e-5
allele num: 64928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.364981e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 3.722e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.802e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.082e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

GenotypeQuality
all individuals: 204
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 671
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540452276788465e-5
allele num: 64916
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.867e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.136e1

DP
type: SiteQuality
SIO_000300: 3.364883e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.502e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.558e0

MQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

GenotypeQuality
all individuals: 3355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33280
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.208057745160219e-4
allele num: 66222
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.534e0

QD
type: SiteQuality
SIO_000300: 1.339e1

FS
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.866323e6

GenotypeQuality
all individuals: 3379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33291
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.937720329024677e-4
allele num: 10212
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508659706716553e-5
allele num: 66284
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.223e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.49e1

DP
type: SiteQuality
SIO_000300: 2.86535e6

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3369
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3479
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66284
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.76e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.223e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.86535e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.49e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33287
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 518
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3492
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3378
bin: 7.75e1
variant carriers: 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: 10220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016864271276435e-5
allele num: 66294
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.847e0

FS
type: SiteQuality
SIO_000300: 8.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.386e1

DP
type: SiteQuality
SIO_000300: 2.864435e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

GenotypeQuality
all individuals: 4107
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3497
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.865273e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.287e0

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2011
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7629
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33288
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4101
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3500
bin: 9.25e1
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: 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: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
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: 2.865917e6

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.297e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.185e0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4036
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 8.75e1
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: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509251713000694e-5
allele num: 66258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 8620
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.372e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: -4.456e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

DP
type: SiteQuality
SIO_000300: 2.867171e6

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.458e0

QD
type: SiteQuality
SIO_000300: 1.683e1

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4058
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.035361966914554e-5
allele num: 65890
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

DP
type: SiteQuality
SIO_000300: 2.878002e6

FS
type: SiteQuality
SIO_000300: 1.684e0

QD
type: SiteQuality
SIO_000300: 1.033e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.404e0

VQSLOD
type: SiteQuality
SIO_000300: -6.578000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 392
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33060
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3506
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7945
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 11566
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 2.843e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.152e0

MQ
type: SiteQuality
SIO_000300: 5.996e1

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

DP
type: SiteQuality
SIO_000300: 2.87839e6

QD
type: SiteQuality
SIO_000300: 1.42e1

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

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

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

GenotypeQuality
all individuals: 228
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33060
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3506
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7945
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516990291262136e-5
allele num: 65920
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.152e0

FS
type: SiteQuality
SIO_000300: 2.843e0

MQ
type: SiteQuality
SIO_000300: 5.996e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.68e0

QD
type: SiteQuality
SIO_000300: 1.42e1

DP
type: SiteQuality
SIO_000300: 2.87839e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

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

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4146
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8066
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2020
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3522
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507567991316408e-5
allele num: 66332
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.986e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 5.418e0

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.528e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

DP
type: SiteQuality
SIO_000300: 2.830234e6

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

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

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4153
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2048
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33190
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50665943470138e-5
allele num: 66372
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.820000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 7.657e0

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.622e-1

DP
type: SiteQuality
SIO_000300: 2.831216e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.548e0

GenotypeQuality
all individuals: 4178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
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: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

FS
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 2.831629e6

QD
type: SiteQuality
SIO_000300: 7.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.326000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3416
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33195
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8360
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.948937828883259e-4
allele num: 10262
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66408
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: 8636
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.036e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 2.176e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.832576e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

VQSLOD
type: SiteQuality
SIO_000300: 8.79e-1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 250
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33191
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.516983859311009e-5
allele num: 66416
num of homozygotes: 1

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.833805e6

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

QD
type: SiteQuality
SIO_000300: 1.892e1

FS
type: SiteQuality
SIO_000300: 4.935e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.43e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.43e-1

GenotypeQuality
all individuals: 4235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3429
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8552
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33195
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3529
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-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

DP
type: SiteQuality
SIO_000300: 2.836152e6

FS
type: SiteQuality
SIO_000300: 4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.12e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.29e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

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

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8618
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3430
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4239
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33210
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2076
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
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: 11
allele frequency: 6.661821705426356e-4
allele num: 16512
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

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: 10370
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.850781e6

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33210
bin: 9.75e1
variant carriers: 100

GenotypeQuality
all individuals: 4239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.892960462873674e-4
allele num: 10370
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 84
allele frequency: 1.261034047919294e-3
allele num: 66612
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.262e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

DP
type: SiteQuality
SIO_000300: 2.850781e6

GenotypeQuality
all individuals: 8646
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4248
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33167
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3416
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 9.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.448e0

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.339e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.826947e6

QD
type: SiteQuality
SIO_000300: 1.209e1

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

GenotypeQuality
all individuals: 3436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2077
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3417
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33167
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 3534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.827451e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

QD
type: SiteQuality
SIO_000300: 1.158e1

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.669e0

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

GenotypeQuality
all individuals: 3439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8649
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2078
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4264
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33166
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.268e1

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 2.827295e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.414e0

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

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33260
bin: 9.75e1
variant carriers: 412

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3532
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8596
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4249
bin: 6.75e1
variant carriers: 1

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
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: 13
allele frequency: 1.122819139747797e-3
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 397
allele frequency: 3.822453302522626e-2
allele num: 10386
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.200048001920077e-4
allele num: 66664
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.87494e6

VQSLOD
type: SiteQuality
SIO_000300: 5.54e0

QD
type: SiteQuality
SIO_000300: 1.322e1

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.219e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 8.75e1
variant carriers: 0

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

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

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: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.0398e1

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.74e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: -1.128e0

DP
type: SiteQuality
SIO_000300: 2.788147e6

QD
type: SiteQuality
SIO_000300: 1.249e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33037
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8596
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2041
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 2.787837e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.435e1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8537
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33037
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
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: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
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: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.327e1

FS
type: SiteQuality
SIO_000300: 1.803e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.788275e6

MQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

GenotypeQuality
all individuals: 4273
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8559
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996641880546894e-5
allele num: 66704
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 2.78725e6

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

QD
type: SiteQuality
SIO_000300: 1.321e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.792e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

GenotypeQuality
all individuals: 33034
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4273
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8559
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 5.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

QD
type: SiteQuality
SIO_000300: 1.321e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.78725e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.792e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

GenotypeQuality
all individuals: 3459
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33030
bin: 9.75e1
variant carriers: 31

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
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: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.249887505624719e-4
allele num: 66670
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.898550724637681e-4
allele num: 10350
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: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.303e1

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.789436e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.865e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8376
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33025
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3556
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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

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: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.951e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

DP
type: SiteQuality
SIO_000300: 2.78023e6

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

QD
type: SiteQuality
SIO_000300: 1.651e1

GenotypeQuality
all individuals: 2045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3557
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.245e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.719e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: -4.86e-2

DP
type: SiteQuality
SIO_000300: 2.780069e6

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

GenotypeQuality
all individuals: 2045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33032
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3450
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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: 66652
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.781153e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.18e0

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33033
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8321
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3560
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3446
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 2.778713e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.423e0

VQSLOD
type: SiteQuality
SIO_000300: -3.65e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.268e1

FS
type: SiteQuality
SIO_000300: 5.192e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33033
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4305
bin: 6.75e1
variant carriers: 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

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: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.683e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 2.778545e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.59e-1

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4298
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33035
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3448
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.76459219172787e-4
allele num: 10348
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: 906
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

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

DP
type: SiteQuality
SIO_000300: 2.778464e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4295
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3449
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8319
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
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 (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
type: SiteQuality
SIO_000300: 2.777182e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.035e0

FS
type: SiteQuality
SIO_000300: 4.078e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.918e0

QD
type: SiteQuality
SIO_000300: 1.319e1

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7915
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2078
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2047
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4225
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33029
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007066606525334e-5
allele num: 66510
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

FS
type: SiteQuality
SIO_000300: 4.268e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.255e0

QD
type: SiteQuality
SIO_000300: 1.368e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

DP
type: SiteQuality
SIO_000300: 2.770787e6

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4183
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33029
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.381e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -2.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.404e0

FS
type: SiteQuality
SIO_000300: 1.4264e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

QD
type: SiteQuality
SIO_000300: 1.46e1

DP
type: SiteQuality
SIO_000300: 2.76478e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.99e1

GenotypeQuality
all individuals: 706
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3422
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7818
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33030
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2071
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.954270080125073e-4
allele num: 10234
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.764358e6

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.291e0

FS
type: SiteQuality
SIO_000300: 5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.097e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3561
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7786
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33029
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.8e-2

DP
type: SiteQuality
SIO_000300: 2.763929e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e0

QD
type: SiteQuality
SIO_000300: 1.194e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33028
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2066
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
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

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

African
type: Population
allele count: 4
allele frequency: 3.911597887737141e-4
allele num: 10226
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 2.763355e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3409
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33023
bin: 9.75e1
variant carriers: 2

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: 11572
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015317814497648e-5
allele num: 66328
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

VQSLOD
type: SiteQuality
SIO_000300: 6.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 3.489e0

DP
type: SiteQuality
SIO_000300: 2.760512e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.426e1

GenotypeQuality
all individuals: 4158
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7523
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3452
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 885
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3405
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33028
bin: 9.75e1
variant carriers: 121

GenotypeQuality
all individuals: 173
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.873062015503876e-4
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 107
allele frequency: 1.236994219653179e-2
allele num: 8650
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508250128201261e-5
allele num: 66302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

QD
type: SiteQuality
SIO_000300: 1.406e1

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 6.57e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

DP
type: SiteQuality
SIO_000300: 2.761547e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e0

GenotypeQuality
all individuals: 4159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3574
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7495
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32960
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2056
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508204633204633e-5
allele num: 66304
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.162e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

DP
type: SiteQuality
SIO_000300: 2.744085e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.26e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7367
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32960
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3461
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.754e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.591e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.704e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.498e0

DP
type: SiteQuality
SIO_000300: 2.742071e6

VQSLOD
type: SiteQuality
SIO_000300: -8.236e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

GenotypeQuality
all individuals: 947
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32961
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3575
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.741078e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 7.607e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.018e1

GenotypeQuality
all individuals: 2050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4121
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3405
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32961
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7305
bin: 6.25e1
variant carriers: 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: 10088
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511487303506651e-5
allele num: 66160
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 7.386e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.59e-1

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 2.740338e6

VQSLOD
type: SiteQuality
SIO_000300: 1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 5.954e1