4-114263024-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263024
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263024
    reference: chr 4
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.30T>C
  hgvsp: ENST00000510275.2:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.157T>C
  hgvsp: ENST00000504415.1:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1111T>C
  hgvsp: ENST00000514960.1:c.1111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3813T>C
  hgvsp: ENST00000503423.1:c.3813T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4074T>C
  hgvsp: ENST00000394537.3:c.4074T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.3975T>C
  hgvsp: ENST00000264366.6:c.3975T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4119T>C
  hgvsp: ENST00000504454.1:c.4119T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1602T>C
  hgvsp: ENST00000509550.1:c.1602T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4074T>C
  hgvsp: ENST00000357077.4:c.4074T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4047T>C
  hgvsp: ENST00000506722.1:c.4047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8262
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1358Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

4-114263034-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263034
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263034
    reference: chr 4
allele count: 3
allele frequency: 2.477577919825579e-5
allele num: 121086
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4084G>C
  hgvsp: ENSP00000349588.4:p.Glu1362Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.40G>C
  hgvsp: ENSP00000421023.2:p.Glu14Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4129G>C
  hgvsp: ENSP00000424722.1:p.Glu1377Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4084G>C
  hgvsp: ENSP00000378044.3:p.Glu1362Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3823G>C
  hgvsp: ENSP00000421011.1:p.Glu1275Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4057G>C
  hgvsp: ENSP00000421067.1:p.Glu1353Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1612G>C
  hgvsp: ENSP00000426944.1:p.Glu538Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.3985G>C
  hgvsp: ENSP00000264366.6:p.Glu1329Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1121G>C
  hgvsp: ENSP00000422853.1:p.Glu375Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.167G>C
  hgvsp: ENSP00000426994.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu1362Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

4-114263051-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263051
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263051
    reference: chr 4
allele count: 1
allele frequency: 8.278282753025713e-6
allele num: 120798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4146G>A
  hgvsp: ENST00000504454.1:c.4146G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.57G>A
  hgvsp: ENST00000510275.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1138G>A
  hgvsp: ENST00000514960.1:c.1138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4002G>A
  hgvsp: ENST00000264366.6:c.4002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4101G>A
  hgvsp: ENST00000357077.4:c.4101G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.184G>A
  hgvsp: ENST00000504415.1:c.184G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4101G>A
  hgvsp: ENST00000394537.3:c.4101G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3840G>A
  hgvsp: ENST00000503423.1:c.3840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1629G>A
  hgvsp: ENST00000509550.1:c.1629G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4074G>A
  hgvsp: ENST00000506722.1:c.4074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7930
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val1367Val
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

4-114263062-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263062
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263062
    reference: chr 4
allele count: 1
allele frequency: 8.311032063961702e-6
allele num: 120322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1149G>T
  hgvsp: ENSP00000422853.1:p.Arg384Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4157G>T
  hgvsp: ENSP00000424722.1:p.Arg1386Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4085G>T
  hgvsp: ENSP00000421067.1:p.Arg1362Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1640G>T
  hgvsp: ENSP00000426944.1:p.Arg547Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4112G>T
  hgvsp: ENSP00000349588.4:p.Arg1371Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.68G>T
  hgvsp: ENSP00000421023.2:p.Arg23Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4013G>T
  hgvsp: ENSP00000264366.6:p.Arg1338Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3851G>T
  hgvsp: ENSP00000421011.1:p.Arg1284Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4112G>T
  hgvsp: ENSP00000378044.3:p.Arg1371Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.195G>T
  hgvsp: ENSP00000426994.1:p.Arg66Met
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1371Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114263069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263069
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263069
    reference: chr 4
allele count: 1
allele frequency: 8.34125752798492e-6
allele num: 119886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3858G>A
  hgvsp: ENST00000503423.1:c.3858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4119G>A
  hgvsp: ENST00000394537.3:c.4119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4092G>A
  hgvsp: ENST00000506722.1:c.4092G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1647G>A
  hgvsp: ENST00000509550.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4119G>A
  hgvsp: ENST00000357077.4:c.4119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4164G>A
  hgvsp: ENST00000504454.1:c.4164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4020G>A
  hgvsp: ENST00000264366.6:c.4020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.75G>A
  hgvsp: ENST00000510275.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1156G>A
  hgvsp: ENST00000514960.1:c.1156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.202G>A
  hgvsp: ENST00000504415.1:c.202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33889
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val1373Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

4-114263069-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263069
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263069
    reference: chr 4
allele count: 1
allele frequency: 8.34125752798492e-6
allele num: 119886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.202G>C
  hgvsp: ENST00000504415.1:c.202G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1647G>C
  hgvsp: ENST00000509550.1:c.1647G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.75G>C
  hgvsp: ENST00000510275.2:c.75G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4119G>C
  hgvsp: ENST00000394537.3:c.4119G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4164G>C
  hgvsp: ENST00000504454.1:c.4164G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1156G>C
  hgvsp: ENST00000514960.1:c.1156G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4092G>C
  hgvsp: ENST00000506722.1:c.4092G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4020G>C
  hgvsp: ENST00000264366.6:c.4020G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4119G>C
  hgvsp: ENST00000357077.4:c.4119G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3858G>C
  hgvsp: ENST00000503423.1:c.3858G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1373Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

4-114263076-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263076
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263076
    reference: chr 4
allele count: 3
allele frequency: 2.523340903356043e-5
allele num: 118890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+4C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+4C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
hgvs: c.4122+4C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/4-114263082-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263082
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263083
    reference: chr 4
allele count: 3
allele frequency: 2.553582676495123e-5
allele num: 117482
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+15dupA
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+15dupA
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8022
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2978
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

4-114263085-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263085
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263085
    reference: chr 4
allele count: 5
allele frequency: 4.296197006409926e-5
allele num: 116382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+13A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+13A>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20308
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4348
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

4-114263085-AAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263085
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263082
    reference: chr 4
allele count: 8
allele frequency: 6.873915210255881e-5
allele num: 116382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+26_4167+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+26_4122+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+26_1650+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+26_3861+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+26_4122+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+26_205+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+26_4095+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+26_4023+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+26_78+28delAAT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+26_1159+28delAAT
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20308
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.75e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AAAT
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-114263087-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263087
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263087
    reference: chr 4
allele count: 1
allele frequency: 8.628276588034307e-6
allele num: 115898
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+15A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+15A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-114263088-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263088
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263088
    reference: chr 4
allele count: 4
allele frequency: 3.455305621782246e-5
allele num: 115764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+16T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+16T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

4-114263090-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263090
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263090
    reference: chr 4
allele count: 11
allele frequency: 9.493725510503512e-5
allele num: 115866
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+18A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+18A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11224
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-114263091-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263091
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263091
    reference: chr 4
allele count: 1
allele frequency: 8.653363562416712e-6
allele num: 115562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+19T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+19T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19888
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

4-114263101-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263101
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263101
    reference: chr 4
allele count: 11263
allele frequency: 9.893362847405221e-2
allele num: 113844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+29T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+29T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.75e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 1.75e1
  variant carriers: 620
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 7.5e0
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.25e1
  variant carriers: 528
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 3.75e1
  variant carriers: 1459
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 2.25e1
  variant carriers: 1122
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 4.75e1
  variant carriers: 806
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 1.25e1
  variant carriers: 258
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 244
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 4.25e1
  variant carriers: 1070
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 15198
  bin: 2.75e1
  variant carriers: 1480
genotype depth: GenotypeDepth
  all individuals: 8289
  bin: 3.25e1
  variant carriers: 1489
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.25e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 98
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 8.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 8637
  bin: 2.25e1
  variant carriers: 13
num of homozygotes: 683
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

4-114263106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263106
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263106
    reference: chr 4
allele count: 25
allele frequency: 2.22182723071454e-4
allele num: 112520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+34C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+34C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

4-114263114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263114
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263114
    reference: chr 4
allele count: 1
allele frequency: 9.042735970195143e-6
allele num: 110586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+42T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+42T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10630
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

4-114263116-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263116
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263116
    reference: chr 4
allele count: 1
allele frequency: 9.092727636436378e-6
allele num: 109978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+44A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+44A>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13290
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3348
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

4-114263119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263119
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263119
    reference: chr 4
allele count: 1
allele frequency: 9.23037161476121e-6
allele num: 108338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+47C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+47C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5573
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-114263124-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114263124
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114263124
    reference: chr 4
allele count: 1
allele frequency: 9.624824346955668e-6
allele num: 103898
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1650+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4023+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3861+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4122+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4122+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4167+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.78+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1159+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4095+52A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+52A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11252
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12878
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-114264142-TTTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264142
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264139
    reference: chr 4
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4123-28_4123-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1073_205+1075delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1160-28_1160-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4024-28_4024-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1651-28_1651-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4168-28_4168-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4123-28_4123-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.79-28_79-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3862-28_3862-26delATT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4096-28_4096-26delATT
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: TTTA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

4-114264152-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264152
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264152
    reference: chr 4
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1160-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4024-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3862-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4168-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1651-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.79-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4123-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1080T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4123-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4096-21T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3707
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21430
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

4-114264154-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264154
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264154
    reference: chr 4
allele count: 34
allele frequency: 2.804910242872228e-4
allele num: 121216
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4168-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1082T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3862-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4024-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.79-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1651-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1160-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4123-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4096-19T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4123-19T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4641
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

4-114264160-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264160
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264160
    reference: chr 4
allele count: 41
allele frequency: 3.381108673780739e-4
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1651-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4123-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3862-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1160-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4168-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4096-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.79-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4123-13T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1088T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4024-13T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

4-114264175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264175
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264175
    reference: chr 4
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4026G>A
  hgvsp: ENST00000264366.6:c.4026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4170G>A
  hgvsp: ENST00000504454.1:c.4170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1653G>A
  hgvsp: ENST00000509550.1:c.1653G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4125G>A
  hgvsp: ENST00000357077.4:c.4125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.81G>A
  hgvsp: ENST00000510275.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4098G>A
  hgvsp: ENST00000506722.1:c.4098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1162G>A
  hgvsp: ENST00000514960.1:c.1162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1103G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4125G>A
  hgvsp: ENST00000394537.3:c.4125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3864G>A
  hgvsp: ENST00000503423.1:c.3864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4125G>A
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

4-114264194-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264194
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264194
    reference: chr 4
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4045T>C
  hgvsp: ENSP00000264366.6:p.Tyr1349His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4144T>C
  hgvsp: ENSP00000378044.3:p.Tyr1382His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1122T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.100T>C
  hgvsp: ENSP00000421023.2:p.Tyr34His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3883T>C
  hgvsp: ENSP00000421011.1:p.Tyr1295His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4144T>C
  hgvsp: ENSP00000349588.4:p.Tyr1382His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1672T>C
  hgvsp: ENSP00000426944.1:p.Tyr558His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1181T>C
  hgvsp: ENSP00000422853.1:p.Tyr395His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4189T>C
  hgvsp: ENSP00000424722.1:p.Tyr1397His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4117T>C
  hgvsp: ENSP00000421067.1:p.Tyr1373His
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr1382His
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

4-114264196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264196
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264196
    reference: chr 4
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4146C>T
  hgvsp: ENST00000357077.4:c.4146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4047C>T
  hgvsp: ENST00000264366.6:c.4047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3885C>T
  hgvsp: ENST00000503423.1:c.3885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1124C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1674C>T
  hgvsp: ENST00000509550.1:c.1674C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4146C>T
  hgvsp: ENST00000394537.3:c.4146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4191C>T
  hgvsp: ENST00000504454.1:c.4191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1183C>T
  hgvsp: ENST00000514960.1:c.1183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.102C>T
  hgvsp: ENST00000510275.2:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4119C>T
  hgvsp: ENST00000506722.1:c.4119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr1382Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

4-114264197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264197
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264197
    reference: chr 4
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1675G>A
  hgvsp: ENSP00000426944.1:p.Val559Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4147G>A
  hgvsp: ENSP00000378044.3:p.Val1383Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4120G>A
  hgvsp: ENSP00000421067.1:p.Val1374Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1184G>A
  hgvsp: ENSP00000422853.1:p.Val396Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3886G>A
  hgvsp: ENSP00000421011.1:p.Val1296Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1125G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.103G>A
  hgvsp: ENSP00000421023.2:p.Val35Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4192G>A
  hgvsp: ENSP00000424722.1:p.Val1398Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4048G>A
  hgvsp: ENSP00000264366.6:p.Val1350Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4147G>A
  hgvsp: ENSP00000349588.4:p.Val1383Ile
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val1383Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114264197-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264197
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264197
    reference: chr 4
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4147G>T
  hgvsp: ENSP00000349588.4:p.Val1383Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4192G>T
  hgvsp: ENSP00000424722.1:p.Val1398Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1184G>T
  hgvsp: ENSP00000422853.1:p.Val396Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1125G>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3886G>T
  hgvsp: ENSP00000421011.1:p.Val1296Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.103G>T
  hgvsp: ENSP00000421023.2:p.Val35Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4120G>T
  hgvsp: ENSP00000421067.1:p.Val1374Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4147G>T
  hgvsp: ENSP00000378044.3:p.Val1383Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1675G>T
  hgvsp: ENSP00000426944.1:p.Val559Phe
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4048G>T
  hgvsp: ENSP00000264366.6:p.Val1350Phe
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7786
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val1383Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

4-114264202-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264202
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264202
    reference: chr 4
allele count: 177
allele frequency: 1.458566813896763e-3
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.108T>C
  hgvsp: ENST00000510275.2:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4125T>C
  hgvsp: ENST00000506722.1:c.4125T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1680T>C
  hgvsp: ENST00000509550.1:c.1680T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4053T>C
  hgvsp: ENST00000264366.6:c.4053T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4197T>C
  hgvsp: ENST00000504454.1:c.4197T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4152T>C
  hgvsp: ENST00000357077.4:c.4152T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1189T>C
  hgvsp: ENST00000514960.1:c.1189T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1130T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3891T>C
  hgvsp: ENST00000503423.1:c.3891T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4152T>C
  hgvsp: ENST00000394537.3:c.4152T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 9.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp1384Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

4-114264208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264208
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264208
    reference: chr 4
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3897C>T
  hgvsp: ENST00000503423.1:c.3897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4158C>T
  hgvsp: ENST00000357077.4:c.4158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1686C>T
  hgvsp: ENST00000509550.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4059C>T
  hgvsp: ENST00000264366.6:c.4059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1136C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1195C>T
  hgvsp: ENST00000514960.1:c.1195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4158C>T
  hgvsp: ENST00000394537.3:c.4158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.114C>T
  hgvsp: ENST00000510275.2:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4203C>T
  hgvsp: ENST00000504454.1:c.4203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4131C>T
  hgvsp: ENST00000506722.1:c.4131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe1386Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

4-114264209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264209
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264209
    reference: chr 4
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3898G>A
  hgvsp: ENSP00000421011.1:p.Gly1300Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4204G>A
  hgvsp: ENSP00000424722.1:p.Gly1402Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1196G>A
  hgvsp: ENSP00000422853.1:p.Gly400Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1137G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4159G>A
  hgvsp: ENSP00000378044.3:p.Gly1387Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4060G>A
  hgvsp: ENSP00000264366.6:p.Gly1354Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1687G>A
  hgvsp: ENSP00000426944.1:p.Gly563Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4132G>A
  hgvsp: ENSP00000421067.1:p.Gly1378Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.115G>A
  hgvsp: ENSP00000421023.2:p.Gly39Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4159G>A
  hgvsp: ENSP00000349588.4:p.Gly1387Ser
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4675
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly1387Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114264218-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264218
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264218
    reference: chr 4
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4141G>T
  hgvsp: ENSP00000421067.1:p.Val1381Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.124G>T
  hgvsp: ENSP00000421023.2:p.Val42Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4168G>T
  hgvsp: ENSP00000349588.4:p.Val1390Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1146G>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1696G>T
  hgvsp: ENSP00000426944.1:p.Val566Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1205G>T
  hgvsp: ENSP00000422853.1:p.Val403Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3907G>T
  hgvsp: ENSP00000421011.1:p.Val1303Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4213G>T
  hgvsp: ENSP00000424722.1:p.Val1405Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4069G>T
  hgvsp: ENSP00000264366.6:p.Val1357Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4168G>T
  hgvsp: ENSP00000378044.3:p.Val1390Leu
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1390Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

4-114264230-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264230
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264230
    reference: chr 4
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.136A>G
  hgvsp: ENSP00000421023.2:p.Lys46Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1158A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4180A>G
  hgvsp: ENSP00000349588.4:p.Lys1394Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4225A>G
  hgvsp: ENSP00000424722.1:p.Lys1409Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4180A>G
  hgvsp: ENSP00000378044.3:p.Lys1394Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1708A>G
  hgvsp: ENSP00000426944.1:p.Lys570Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4081A>G
  hgvsp: ENSP00000264366.6:p.Lys1361Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1217A>G
  hgvsp: ENSP00000422853.1:p.Lys407Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3919A>G
  hgvsp: ENSP00000421011.1:p.Lys1307Glu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4153A>G
  hgvsp: ENSP00000421067.1:p.Lys1385Glu
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys1394Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

4-114264242-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264242
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264242
    reference: chr 4
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1170C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1720C>T
  hgvsp: ENSP00000426944.1:p.His574Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1229C>T
  hgvsp: ENSP00000422853.1:p.His411Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3931C>T
  hgvsp: ENSP00000421011.1:p.His1311Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4165C>T
  hgvsp: ENSP00000421067.1:p.His1389Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4093C>T
  hgvsp: ENSP00000264366.6:p.His1365Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.148C>T
  hgvsp: ENSP00000421023.2:p.His50Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4192C>T
  hgvsp: ENSP00000349588.4:p.His1398Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4237C>T
  hgvsp: ENSP00000424722.1:p.His1413Tyr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4192C>T
  hgvsp: ENSP00000378044.3:p.His1398Tyr
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19598
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His1398Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

4-114264255-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264255
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264256
    reference: chr 4
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4257dupT
  hgvsp: ENSP00000424722.1:p.Ala1420CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4212dupT
  hgvsp: ENSP00000349588.4:p.Ala1405CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4212dupT
  hgvsp: ENSP00000378044.3:p.Ala1405CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.168dupT
  hgvsp: ENSP00000421023.2:p.Ala57CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1740dupT
  hgvsp: ENSP00000426944.1:p.Ala581CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1249dupT
  hgvsp: ENSP00000422853.1:p.Ala418CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1190dupT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4185dupT
  hgvsp: ENSP00000421067.1:p.Ala1396CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3951dupT
  hgvsp: ENSP00000421011.1:p.Ala1318CysfsTer6
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4113dupT
  hgvsp: ENSP00000264366.6:p.Ala1372CysfsTer6
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala1405CysfsTer6
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

4-114264256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264256
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264256
    reference: chr 4
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1243T>C
  hgvsp: ENST00000514960.1:c.1243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1184T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4206T>C
  hgvsp: ENST00000394537.3:c.4206T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4206T>C
  hgvsp: ENST00000357077.4:c.4206T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3945T>C
  hgvsp: ENST00000503423.1:c.3945T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4107T>C
  hgvsp: ENST00000264366.6:c.4107T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1734T>C
  hgvsp: ENST00000509550.1:c.1734T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4251T>C
  hgvsp: ENST00000504454.1:c.4251T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4179T>C
  hgvsp: ENST00000506722.1:c.4179T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.162T>C
  hgvsp: ENST00000510275.2:c.162T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser1402Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

4-114264268-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264268
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264268
    reference: chr 4
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1746C>T
  hgvsp: ENST00000509550.1:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4263C>T
  hgvsp: ENST00000504454.1:c.4263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4218C>T
  hgvsp: ENST00000394537.3:c.4218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4119C>T
  hgvsp: ENST00000264366.6:c.4119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1255C>T
  hgvsp: ENST00000514960.1:c.1255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1196C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4218C>T
  hgvsp: ENST00000357077.4:c.4218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4191C>T
  hgvsp: ENST00000506722.1:c.4191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3957C>T
  hgvsp: ENST00000503423.1:c.3957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.174C>T
  hgvsp: ENST00000510275.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe1406Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum

4-114264270-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264270
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264270
    reference: chr 4
allele count: 15
allele frequency: 1.23758291805551e-4
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1257A>G
  hgvsp: ENSP00000422853.1:p.Lys420Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3959A>G
  hgvsp: ENSP00000421011.1:p.Lys1320Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1748A>G
  hgvsp: ENSP00000426944.1:p.Lys583Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4121A>G
  hgvsp: ENSP00000264366.6:p.Lys1374Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4193A>G
  hgvsp: ENSP00000421067.1:p.Lys1398Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.176A>G
  hgvsp: ENSP00000421023.2:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4265A>G
  hgvsp: ENSP00000424722.1:p.Lys1422Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4220A>G
  hgvsp: ENSP00000378044.3:p.Lys1407Arg
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1198A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4220A>G
  hgvsp: ENSP00000349588.4:p.Lys1407Arg
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys1407Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

4-114264289-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264289
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264289
    reference: chr 4
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4212A>G
  hgvsp: ENST00000506722.1:c.4212A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1276A>G
  hgvsp: ENST00000514960.1:c.1276A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4284A>G
  hgvsp: ENST00000504454.1:c.4284A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4239A>G
  hgvsp: ENST00000357077.4:c.4239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1767A>G
  hgvsp: ENST00000509550.1:c.1767A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4140A>G
  hgvsp: ENST00000264366.6:c.4140A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1217A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3978A>G
  hgvsp: ENST00000503423.1:c.3978A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4239A>G
  hgvsp: ENST00000394537.3:c.4239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.195A>G
  hgvsp: ENST00000510275.2:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu1413Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

4-114264295-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264295
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264295
    reference: chr 4
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1282C>G
  hgvsp: ENST00000514960.1:c.1282C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1223C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4245C>G
  hgvsp: ENST00000394537.3:c.4245C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4245C>G
  hgvsp: ENST00000357077.4:c.4245C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4290C>G
  hgvsp: ENST00000504454.1:c.4290C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4146C>G
  hgvsp: ENST00000264366.6:c.4146C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1773C>G
  hgvsp: ENST00000509550.1:c.1773C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3984C>G
  hgvsp: ENST00000503423.1:c.3984C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.201C>G
  hgvsp: ENST00000510275.2:c.201C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4218C>G
  hgvsp: ENST00000506722.1:c.4218C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val1415Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

4-114264305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264305
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264305
    reference: chr 4
allele count: 2
allele frequency: 1.656012983141788e-5
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+7T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1233T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 2.25e1
  variant carriers: 0
hgvs: c.4248+7T>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/4-114264310-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264310
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264310
    reference: chr 4
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1238A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+12A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+12A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-114264323-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264323
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264323
    reference: chr 4
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1251A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+25A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+25A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17373
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

4-114264324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264324
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264324
    reference: chr 4
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1252T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+26T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+26T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17103
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7040
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

4-114264330-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264330
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264330
    reference: chr 4
allele count: 1
allele frequency: 8.307579835842223e-6
allele num: 120372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1258T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+32T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+32T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16969
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

4-114264331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264331
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264331
    reference: chr 4
allele count: 1
allele frequency: 8.307993951780402e-6
allele num: 120366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1259T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+33T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+33T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16148
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/4-114264346-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114264346
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114264346
    reference: chr 4
allele count: 1
allele frequency: 8.346548702111677e-6
allele num: 119810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4293+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.205+1274C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1776+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.204+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3987+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4248+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4221+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1285+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4248+48C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4149+48C>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15070
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

4-114267006-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267006
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267006
    reference: chr 4
allele count: 2
allele frequency: 1.650301179965344e-5
allele num: 121190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-50A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-50A>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-114267021-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267021
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267020
    reference: chr 4
allele count: 2
allele frequency: 1.649892756970797e-5
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-34delT
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-34delT
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: AT
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

4-114267023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267023
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267023
    reference: chr 4
allele count: 121296
allele frequency: 9.997856942681459e-1
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-33G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-33G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.25e1
  variant carriers: 2736
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 8.75e1
  variant carriers: 3109
genotype depth: GenotypeDepth
  all individuals: 12754
  bin: 9.75e1
  variant carriers: 12754
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 5.25e1
  variant carriers: 4126
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 9.25e1
  variant carriers: 2426
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 2.75e1
  variant carriers: 841
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 5.75e1
  variant carriers: 4586
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 4.75e1
  variant carriers: 3337
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 7.75e1
  variant carriers: 4352
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 1395
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.25e1
  variant carriers: 434
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 4940
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 7.25e1
  variant carriers: 4727
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 1932
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 8.25e1
  variant carriers: 3769
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 6.25e1
  variant carriers: 4915
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 58539
  bin: 9.75e1
  variant carriers: 58539
num of homozygotes: 60635
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-114267035-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267035
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267035
    reference: chr 4
allele count: 2429
allele frequency: 2.002902518264426e-2
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-21T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-21T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 8.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 6.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 6.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 5.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 9.25e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 9.75e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 7.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 5.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 218
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2737
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 267
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum

4-114267035-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267035
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267035
    reference: chr 4
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-21T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-21T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

4-114267036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267036
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267036
    reference: chr 4
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-20G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-20G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

4-114267046-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267046
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267046
    reference: chr 4
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777-10C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249-10C>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

4-114267056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267056
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267056
    reference: chr 4
allele count: 3
allele frequency: 2.473288484368817e-5
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4249G>A
  hgvsp: ENSP00000349588.4:p.Val1417Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4222G>A
  hgvsp: ENSP00000421067.1:p.Val1408Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3988G>A
  hgvsp: ENSP00000421011.1:p.Val1330Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4150G>A
  hgvsp: ENSP00000264366.6:p.Val1384Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1777G>A
  hgvsp: ENSP00000426944.1:p.Val593Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.206G>A
  hgvsp: ENSP00000426994.1:p.Val70Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4294G>A
  hgvsp: ENSP00000424722.1:p.Val1432Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.205G>A
  hgvsp: ENSP00000421023.2:p.Val69Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1286G>A
  hgvsp: ENSP00000422853.1:p.Val430Ile
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4249G>A
  hgvsp: ENSP00000378044.3:p.Val1417Ile
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1417Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114267059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267059
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267059
    reference: chr 4
allele count: 4
allele frequency: 3.297663605335619e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.208C>T
  hgvsp: ENSP00000421023.2:p.Arg70Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4153C>T
  hgvsp: ENSP00000264366.6:p.Arg1385Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4297C>T
  hgvsp: ENSP00000424722.1:p.Arg1433Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1289C>T
  hgvsp: ENSP00000422853.1:p.Arg431Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1780C>T
  hgvsp: ENSP00000426944.1:p.Arg594Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.209C>T
  hgvsp: ENSP00000426994.1:p.Arg71Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4252C>T
  hgvsp: ENSP00000378044.3:p.Arg1418Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4252C>T
  hgvsp: ENSP00000349588.4:p.Arg1418Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3991C>T
  hgvsp: ENSP00000421011.1:p.Arg1331Cys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4225C>T
  hgvsp: ENSP00000421067.1:p.Arg1409Cys
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg1418Cys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

4-114267060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267060
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267060
    reference: chr 4
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3992G>A
  hgvsp: ENSP00000421011.1:p.Arg1331His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.209G>A
  hgvsp: ENSP00000421023.2:p.Arg70His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.210G>A
  hgvsp: ENSP00000426994.1:p.Arg71His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1290G>A
  hgvsp: ENSP00000422853.1:p.Arg431His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4298G>A
  hgvsp: ENSP00000424722.1:p.Arg1433His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4154G>A
  hgvsp: ENSP00000264366.6:p.Arg1385His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1781G>A
  hgvsp: ENSP00000426944.1:p.Arg594His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4226G>A
  hgvsp: ENSP00000421067.1:p.Arg1409His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4253G>A
  hgvsp: ENSP00000378044.3:p.Arg1418His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4253G>A
  hgvsp: ENSP00000349588.4:p.Arg1418His
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1418His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-114267061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267061
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267061
    reference: chr 4
allele count: 4
allele frequency: 3.297554863069035e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4254C>T
  hgvsp: ENST00000357077.4:c.4254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.211C>T
  hgvsp: ENST00000504415.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.210C>T
  hgvsp: ENST00000510275.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3993C>T
  hgvsp: ENST00000503423.1:c.3993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4227C>T
  hgvsp: ENST00000506722.1:c.4227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1782C>T
  hgvsp: ENST00000509550.1:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4155C>T
  hgvsp: ENST00000264366.6:c.4155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4299C>T
  hgvsp: ENST00000504454.1:c.4299C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4254C>T
  hgvsp: ENST00000394537.3:c.4254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1291C>T
  hgvsp: ENST00000514960.1:c.1291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1418Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

4-114267062-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267062
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267062
    reference: chr 4
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3994G>C
  hgvsp: ENSP00000421011.1:p.Asp1332His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4228G>C
  hgvsp: ENSP00000421067.1:p.Asp1410His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4156G>C
  hgvsp: ENSP00000264366.6:p.Asp1386His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1292G>C
  hgvsp: ENSP00000422853.1:p.Asp432His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4255G>C
  hgvsp: ENSP00000378044.3:p.Asp1419His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.212G>C
  hgvsp: ENSP00000426994.1:p.Asp72His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4300G>C
  hgvsp: ENSP00000424722.1:p.Asp1434His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4255G>C
  hgvsp: ENSP00000349588.4:p.Asp1419His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1783G>C
  hgvsp: ENSP00000426944.1:p.Asp595His
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.211G>C
  hgvsp: ENSP00000421023.2:p.Asp71His
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp1419His
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

4-114267066-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267066
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267066
    reference: chr 4
allele count: 13
allele frequency: 1.071723000824402e-4
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1787C>T
  hgvsp: ENSP00000426944.1:p.Thr596Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.216C>T
  hgvsp: ENSP00000426994.1:p.Thr73Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4259C>T
  hgvsp: ENSP00000349588.4:p.Thr1420Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.215C>T
  hgvsp: ENSP00000421023.2:p.Thr72Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4304C>T
  hgvsp: ENSP00000424722.1:p.Thr1435Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3998C>T
  hgvsp: ENSP00000421011.1:p.Thr1333Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1296C>T
  hgvsp: ENSP00000422853.1:p.Thr433Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4232C>T
  hgvsp: ENSP00000421067.1:p.Thr1411Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4160C>T
  hgvsp: ENSP00000264366.6:p.Thr1387Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4259C>T
  hgvsp: ENSP00000378044.3:p.Thr1420Met
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr1420Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

4-114267067-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267067
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267067
    reference: chr 4
allele count: 7
allele frequency: 5.771006463527239e-5
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4260G>A
  hgvsp: ENST00000394537.3:c.4260G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4233G>A
  hgvsp: ENST00000506722.1:c.4233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4305G>A
  hgvsp: ENST00000504454.1:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.216G>A
  hgvsp: ENST00000510275.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1297G>A
  hgvsp: ENST00000514960.1:c.1297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3999G>A
  hgvsp: ENST00000503423.1:c.3999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.217G>A
  hgvsp: ENST00000504415.1:c.217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4260G>A
  hgvsp: ENST00000357077.4:c.4260G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1788G>A
  hgvsp: ENST00000509550.1:c.1788G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4161G>A
  hgvsp: ENST00000264366.6:c.4161G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr1420Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-114267067-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267067
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267067
    reference: chr 4
allele count: 6
allele frequency: 4.946576968737634e-5
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.216G>T
  hgvsp: ENST00000510275.2:c.216G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4305G>T
  hgvsp: ENST00000504454.1:c.4305G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4260G>T
  hgvsp: ENST00000394537.3:c.4260G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4233G>T
  hgvsp: ENST00000506722.1:c.4233G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1297G>T
  hgvsp: ENST00000514960.1:c.1297G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4161G>T
  hgvsp: ENST00000264366.6:c.4161G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.3999G>T
  hgvsp: ENST00000503423.1:c.3999G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4260G>T
  hgvsp: ENST00000357077.4:c.4260G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.217G>T
  hgvsp: ENST00000504415.1:c.217G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1788G>T
  hgvsp: ENST00000509550.1:c.1788G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr1420Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

4-114267077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267077
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267077
    reference: chr 4
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1307C>T
  hgvsp: ENSP00000422853.1:p.Pro437Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4171C>T
  hgvsp: ENSP00000264366.6:p.Pro1391Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4270C>T
  hgvsp: ENSP00000378044.3:p.Pro1424Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4270C>T
  hgvsp: ENSP00000349588.4:p.Pro1424Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.226C>T
  hgvsp: ENSP00000421023.2:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.227C>T
  hgvsp: ENSP00000426994.1:p.Pro77Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.4009C>T
  hgvsp: ENSP00000421011.1:p.Pro1337Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4315C>T
  hgvsp: ENSP00000424722.1:p.Pro1439Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1798C>T
  hgvsp: ENSP00000426944.1:p.Pro600Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4243C>T
  hgvsp: ENSP00000421067.1:p.Pro1415Ser
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro1424Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

4-114267082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267082
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267082
    reference: chr 4
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4275C>T
  hgvsp: ENST00000394537.3:c.4275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.231C>T
  hgvsp: ENST00000510275.2:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1803C>T
  hgvsp: ENST00000509550.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.4014C>T
  hgvsp: ENST00000503423.1:c.4014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4176C>T
  hgvsp: ENST00000264366.6:c.4176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4275C>T
  hgvsp: ENST00000357077.4:c.4275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4320C>T
  hgvsp: ENST00000504454.1:c.4320C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4248C>T
  hgvsp: ENST00000506722.1:c.4248C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1312C>T
  hgvsp: ENST00000514960.1:c.1312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.232C>T
  hgvsp: ENST00000504415.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys1425Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

4-114267086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267086
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267086
    reference: chr 4
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1316C>T
  hgvsp: ENSP00000422853.1:p.Arg440Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.4018C>T
  hgvsp: ENSP00000421011.1:p.Arg1340Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4252C>T
  hgvsp: ENSP00000421067.1:p.Arg1418Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.235C>T
  hgvsp: ENSP00000421023.2:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4279C>T
  hgvsp: ENSP00000378044.3:p.Arg1427Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4180C>T
  hgvsp: ENSP00000264366.6:p.Arg1394Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.236C>T
  hgvsp: ENSP00000426994.1:p.Arg80Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4324C>T
  hgvsp: ENSP00000424722.1:p.Arg1442Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1807C>T
  hgvsp: ENSP00000426944.1:p.Arg603Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4279C>T
  hgvsp: ENSP00000349588.4:p.Arg1427Ter
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3065
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg1427Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-114267088-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267088
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267088
    reference: chr 4
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1809A>G
  hgvsp: ENST00000509550.1:c.1809A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.237A>G
  hgvsp: ENST00000510275.2:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4281A>G
  hgvsp: ENST00000394537.3:c.4281A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.4020A>G
  hgvsp: ENST00000503423.1:c.4020A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.238A>G
  hgvsp: ENST00000504415.1:c.238A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4326A>G
  hgvsp: ENST00000504454.1:c.4326A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1318A>G
  hgvsp: ENST00000514960.1:c.1318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4182A>G
  hgvsp: ENST00000264366.6:c.4182A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4281A>G
  hgvsp: ENST00000357077.4:c.4281A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4254A>G
  hgvsp: ENST00000506722.1:c.4254A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1427Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

4-114267094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267094
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267094
    reference: chr 4
allele count: 9
allele frequency: 7.420110147412856e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4287A>G
  hgvsp: ENST00000394537.3:c.4287A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4188A>G
  hgvsp: ENST00000264366.6:c.4188A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4287A>G
  hgvsp: ENST00000357077.4:c.4287A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1324A>G
  hgvsp: ENST00000514960.1:c.1324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1815A>G
  hgvsp: ENST00000509550.1:c.1815A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4332A>G
  hgvsp: ENST00000504454.1:c.4332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.243A>G
  hgvsp: ENST00000510275.2:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4260A>G
  hgvsp: ENST00000506722.1:c.4260A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.244A>G
  hgvsp: ENST00000504415.1:c.244A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.4026A>G
  hgvsp: ENST00000503423.1:c.4026A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser1429Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

4-114267098-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114267098
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114267098
    reference: chr 4
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000424722
  ensembl transcript: ENST00000504454
  gene symbol: ANK2
  hgvsc: ENST00000504454.1:c.4336A>G
  hgvsp: ENSP00000424722.1:p.Met1446Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.247A>G
  hgvsp: ENSP00000421023.2:p.Met83Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1819A>G
  hgvsp: ENSP00000426944.1:p.Met607Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4264A>G
  hgvsp: ENSP00000421067.1:p.Met1422Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422853
  ensembl transcript: ENST00000514960
  gene symbol: ANK2
  hgvsc: ENST00000514960.1:c.1328A>G
  hgvsp: ENSP00000422853.1:p.Met444Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4291A>G
  hgvsp: ENSP00000378044.3:p.Met1431Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.4192A>G
  hgvsp: ENSP00000264366.6:p.Met1398Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421011
  ensembl transcript: ENST00000503423
  gene symbol: ANK2
  hgvsc: ENST00000503423.1:c.4030A>G
  hgvsp: ENSP00000421011.1:p.Met1344Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.4291A>G
  hgvsp: ENSP00000349588.4:p.Met1431Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426994
  ensembl transcript: ENST00000504415
  gene symbol: ANK2
  hgvsc: ENST00000504415.1:c.248A>G
  hgvsp: ENSP00000426994.1:p.Met84Val
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met1431Val
num of homozygotes: 0
reference allele: A

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

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

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35139
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1896
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7934
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1382
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 8.013e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.987e1

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 1.982329e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.695e0

QD
type: SiteQuality
SIO_000300: 1.178e1

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8236
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2618
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1892
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7935
bin: 9.75e1
variant carriers: 3

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: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005168890491646e-5
allele num: 66552
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.266e0

DP
type: SiteQuality
SIO_000300: 1.980007e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.792e0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e-1

QD
type: SiteQuality
SIO_000300: 1.632e1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

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

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

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1379
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
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: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 1.974778e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.293e0

QD
type: SiteQuality
SIO_000300: 1.685e1

VQSLOD
type: SiteQuality
SIO_000300: -6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.326e0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2573
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1378
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8102
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2152
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7928
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34197
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.439e0

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

DP
type: SiteQuality
SIO_000300: 1.967152e6

QD
type: SiteQuality
SIO_000300: 1.631e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.226e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1876
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GenotypeQuality
all individuals: 2143
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65918
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.49e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.285e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 1.960967e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65918
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 1.285e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
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SIO_000300: 4.49e-1

DP
type: SiteQuality
SIO_000300: 1.960967e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 1.214e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.829491401390413e-4
allele num: 16398
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.944708e6

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.003e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.640801930573603e-5
allele num: 64644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.04e-1

DP
type: SiteQuality
SIO_000300: 1.914079e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

FS
type: SiteQuality
SIO_000300: 2.433e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 2.964e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64046
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

East Asian
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allele frequency: 6.270378730875344e-4
allele num: 7974
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.09e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 1.874032e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

FS
type: SiteQuality
SIO_000300: 2.724e0

QD
type: SiteQuality
SIO_000300: 6.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.530924678505818e-4
allele num: 6532
num of homozygotes: 0

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

South Asian
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allele frequency: 6.161429451632779e-5
allele num: 16230
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.368266558411141e-5
allele num: 64046
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.874032e6

FS
type: SiteQuality
SIO_000300: 2.724e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 6.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63780
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.069976460517869e-4
allele num: 9346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

Other
type: Population
allele count: 0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 2.846e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.847298e6

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.37e0

QD
type: SiteQuality
SIO_000300: 1.147e1

MQ
type: SiteQuality
SIO_000300: 5.841e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.140900810352409e-5
allele num: 63676
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.775883502042266e-4
allele num: 11262
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 874
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.364e0

GenotypeQuality
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1782
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7881
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 6566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5147
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.533742331288344e-3
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56843062831331e-5
allele num: 63758
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.842161e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

QD
type: SiteQuality
SIO_000300: 1.942e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5495
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
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GenotypeQuality
all individuals: 27675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7869
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.174364040503828e-5
allele num: 16196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63564
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

QD
type: SiteQuality
SIO_000300: 1.499e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.831096e6

GenotypeQuality
all individuals: 2302
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1135
bin: 7.25e1
variant carriers: 32

GenotypeQuality
all individuals: 1433
bin: 7.75e1
variant carriers: 55

GenotypeQuality
all individuals: 1511
bin: 3.75e1
variant carriers: 13

GenotypeQuality
all individuals: 402
bin: 4.75e1
variant carriers: 21

GenotypeQuality
all individuals: 2770
bin: 3.25e1
variant carriers: 13

GenotypeQuality
all individuals: 227
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 277
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 247
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 18326
bin: 6.25e1
variant carriers: 28

GenotypeQuality
all individuals: 1020
bin: 8.25e1
variant carriers: 37

GenotypeQuality
all individuals: 3938
bin: 6.75e1
variant carriers: 38

GenotypeQuality
all individuals: 14882
bin: 9.75e1
variant carriers: 10268

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 57

GenotypeQuality
all individuals: 361
bin: 5.25e1
variant carriers: 26

GenotypeQuality
all individuals: 559
bin: 5.75e1
variant carriers: 29

Other
type: Population
allele count: 94
allele frequency: 1.077981651376147e-1
allele num: 872
num of homozygotes: 5

African
type: Population
allele count: 196
allele frequency: 2.158114952653601e-2
allele num: 9082
num of homozygotes: 6

Latino
type: Population
allele count: 655
allele frequency: 5.893467698398416e-2
allele num: 11114
num of homozygotes: 23

European (Finnish)
type: Population
allele count: 768
allele frequency: 1.186650185414092e-1
allele num: 6472
num of homozygotes: 42

South Asian
type: Population
allele count: 1044
allele frequency: 6.499813223757937e-2
allele num: 16062
num of homozygotes: 47

East Asian
type: Population
allele count: 3
allele frequency: 3.904216553878188e-4
allele num: 7684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8503
allele frequency: 1.35921864509735e-1
allele num: 62558
num of homozygotes: 560

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

DP
type: SiteQuality
SIO_000300: 1.73282e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

QD
type: SiteQuality
SIO_000300: 1.817e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.67e0

GenotypeQuality
all individuals: 1363
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4324
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10637
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5602
bin: 9.75e1
variant carriers: 25

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.566808723990975e-3
allele num: 15956
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.209e0

DP
type: SiteQuality
SIO_000300: 1.556615e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.288e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

GenotypeQuality
all individuals: 1626
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13631
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4710
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5575
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3540
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6247
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.165902841429881e-5
allele num: 10910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15832
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.405e1

DP
type: SiteQuality
SIO_000300: 1.461325e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.012e-1

MQ
type: SiteQuality
SIO_000300: 5.879e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

GenotypeQuality
all individuals: 950
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1953
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5576
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6500
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.661405549094534e-5
allele num: 60190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.747e1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

QD
type: SiteQuality
SIO_000300: 8.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.453e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

FS
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 1.44585e6

GenotypeQuality
all individuals: 1129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6672
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9575
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2487
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5857
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15644
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.40331181588549e-4
allele num: 7126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10754
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.256e0

QD
type: SiteQuality
SIO_000300: 2.097e1

VQSLOD
type: SiteQuality
SIO_000300: -1.939e0

DP
type: SiteQuality
SIO_000300: 1.426963e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

GenotypeQuality
all individuals: 1402
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6724
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5569
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3872
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6086
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6710
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2780
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4830
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.57670944263551e-5
allele num: 10442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56612
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.57e0

VQSLOD
type: SiteQuality
SIO_000300: -1.458e0

DP
type: SiteQuality
SIO_000300: 1.410862e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Finnish)
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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: 8598
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

MQRankSum
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SIO_000300: -5.82e-1

MQ
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SIO_000300: 5.728e1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 7.519e0

ReadPosRankSum
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SIO_000300: 5.81e-1

BaseQRankSum
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SIO_000300: 4.83e-1

DP
type: SiteQuality
SIO_000300: 2.314367e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 1.797e1

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

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

Latino
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allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

European (Finnish)
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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

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.272e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -1.734e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.85e0

DP
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SIO_000300: 2.316093e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 1.664e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 34

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.93012931866435e-4
allele num: 10362
num of homozygotes: 0

European (Finnish)
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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)
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allele count: 29
allele frequency: 4.35043504350435e-4
allele num: 66660
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
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SIO_000300: 5.978e1

VQSLOD
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -5.0e-4

BaseQRankSum
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DP
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SIO_000300: 2.31758e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 41

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

Latino
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allele count: 41
allele frequency: 3.544872903337368e-3
allele num: 11566
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

ReadPosRankSum
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SIO_000300: 7.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

DP
type: SiteQuality
SIO_000300: 2.318096e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.44e-1

QD
type: SiteQuality
SIO_000300: 1.35e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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FS
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SIO_000300: 5.4e-1

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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QD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Other
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European (Non-Finnish)
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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DP
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

East Asian
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InbreedingCoeff
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SIO_000300: 8.3e-3

VQSLOD
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SIO_000300: 2.02e-1

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.212e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.823e0

DP
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SIO_000300: 2.316592e6

MQRankSum
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SIO_000300: 8.61e-1

ClippingRankSum
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SIO_000300: -1.131e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
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South Asian
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ClippingRankSum
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VQSLOD
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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SIO_000300: 8.3e-3

GenotypeQuality
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variant carriers: 177

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.09851005785892e-4
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num of homozygotes: 0

African
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allele num: 10400
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East Asian
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South Asian
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allele frequency: 4.239854633555421e-3
allele num: 16510
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Latino
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Other
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66710
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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FS
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SIO_000300: 1.727e0

BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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DP
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MQ
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SIO_000300: 5.968e1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

East Asian
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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QD
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FS
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66704
num of homozygotes: 0

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

European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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DP
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FS
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

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

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

European (Finnish)
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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: 66668
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

QD
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

FS
type: SiteQuality
SIO_000300: 1.085e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.3112e6

VQSLOD
type: SiteQuality
SIO_000300: -1.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
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: 906
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e0

VQSLOD
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SIO_000300: 1.2e0

DP
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SIO_000300: 2.310563e6

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.226e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

QD
type: SiteQuality
SIO_000300: 1.281e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 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: 11560
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 2.307673e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 8.28e-1

FS
type: SiteQuality
SIO_000300: 6.139e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.545454545454545e-4
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.65090799939967e-4
allele num: 66630
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.307192e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 2.763e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

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

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
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: 6598
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.601e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

QD
type: SiteQuality
SIO_000300: 1.598e1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 2.301171e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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: 1
allele frequency: 1.504257047444267e-5
allele num: 66478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.84e-1

MQ
type: SiteQuality
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FS
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ReadPosRankSum
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SIO_000300: 7.44e-1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.297621e6

QD
type: SiteQuality
SIO_000300: 1.495e1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.167133520074697e-4
allele num: 8568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506568639267205e-5
allele num: 66376
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508159140952553e-5
allele num: 66306
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
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: 902
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510026576467746e-5
allele num: 66224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.25341e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
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: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66154
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.085e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.576e0

MQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

DP
type: SiteQuality
SIO_000300: 2.222932e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2598
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66148
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
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: 8498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.363e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: -2.526e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.222655e6

QD
type: SiteQuality
SIO_000300: 1.483e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 6.235e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.349e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e-1

DP
type: SiteQuality
SIO_000300: 2.154105e6

QD
type: SiteQuality
SIO_000300: 1.105e1

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

GenotypeQuality
all individuals: 145
bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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: 2
allele frequency: 3.001020346917952e-5
allele num: 66644
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: 16504
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.525e0

FS
type: SiteQuality
SIO_000300: 4.424e0

DP
type: SiteQuality
SIO_000300: 3.642644e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.6e1

FS
type: SiteQuality
SIO_000300: 2.738e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

DP
type: SiteQuality
SIO_000300: 3.646699e6

GenotypeQuality
all individuals: 369
bin: 8.25e1
variant carriers: 369

GenotypeQuality
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bin: 7.25e1
variant carriers: 122

GenotypeQuality
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bin: 4.75e1
variant carriers: 64

GenotypeQuality
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variant carriers: 55

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 17

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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variant carriers: 20

GenotypeQuality
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variant carriers: 43

GenotypeQuality
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variant carriers: 259

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 240

GenotypeQuality
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variant carriers: 515

GenotypeQuality
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bin: 6.25e1
variant carriers: 141

GenotypeQuality
all individuals: 186
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variant carriers: 186

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 77

East Asian
type: Population
allele count: 8630
allele frequency: 1.0e0
allele num: 8630
num of homozygotes: 4315

European (Finnish)
type: Population
allele count: 6612
allele frequency: 1.0e0
allele num: 6612
num of homozygotes: 3306

Other
type: Population
allele count: 908
allele frequency: 1.0e0
allele num: 908
num of homozygotes: 454

African
type: Population
allele count: 10403
allele frequency: 9.999038831218762e-1
allele num: 10404
num of homozygotes: 5201

Latino
type: Population
allele count: 11547
allele frequency: 9.999134049186006e-1
allele num: 11548
num of homozygotes: 5773

South Asian
type: Population
allele count: 16508
allele frequency: 1.0e0
allele num: 16508
num of homozygotes: 8254

European (Non-Finnish)
type: Population
allele count: 66688
allele frequency: 9.996402446336491e-1
allele num: 66712
num of homozygotes: 33332

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 4.693252e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

QD
type: SiteQuality
SIO_000300: 3.294e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 2169
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1163
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 2400
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GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45686
bin: 9.75e1
variant carriers: 2154

GenotypeQuality
all individuals: 2865
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 2333
allele frequency: 2.023768216516308e-1
allele num: 11528
num of homozygotes: 266

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

African
type: Population
allele count: 26
allele frequency: 2.499038831218762e-3
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 48
allele frequency: 5.569737758180552e-3
allele num: 8618
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.398728673802884e-4
allele num: 66702
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.531476e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.594e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.938e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.91e0

FS
type: SiteQuality
SIO_000300: 5.81e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

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

GenotypeQuality
all individuals: 2169
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2737
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45686
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2400
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.91e0

DP
type: SiteQuality
SIO_000300: 3.531476e6

FS
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.938e-1

QD
type: SiteQuality
SIO_000300: 1.594e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 45351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1185
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1459
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2807
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 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: 16506
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.878e0

QD
type: SiteQuality
SIO_000300: 1.199e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-1

MQ
type: SiteQuality
SIO_000300: 5.806e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

DP
type: SiteQuality
SIO_000300: 3.483275e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

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

GenotypeQuality
all individuals: 2458
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2998
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2209
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 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: 66702
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: 10404
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.242e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.613e0

DP
type: SiteQuality
SIO_000300: 3.483609e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

GenotypeDepth
all individuals: 6760
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45340
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1462
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2461
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49748141041017e-5
allele num: 66704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 1.144e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 3.48393e6

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.91e-1

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

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

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

GenotypeQuality
all individuals: 2014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3009
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45339
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 1192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
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: 11540
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49734656552634e-5
allele num: 66706
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.095e0

FS
type: SiteQuality
SIO_000300: 1.141e0

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.55e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.97e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 3.483915e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

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

GenotypeQuality
all individuals: 2016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45338
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2803
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 11540
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.169e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

FS
type: SiteQuality
SIO_000300: 8.427e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.706e1

VQSLOD
type: SiteQuality
SIO_000300: -9.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.47e-1

QD
type: SiteQuality
SIO_000300: 1.919e1

DP
type: SiteQuality
SIO_000300: 3.48385e6

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 1461
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 2211
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2803
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45335
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998231043684226e-5
allele num: 66706
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.598e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

FS
type: SiteQuality
SIO_000300: 8.843999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 3.483941e6

MQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.235e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

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

VQSLOD
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SIO_000300: -1.497e0

MQ
type: SiteQuality
SIO_000300: 5.823e1

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

FS
type: SiteQuality
SIO_000300: 1.004e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

DP
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SIO_000300: 3.483878e6

MQRankSum
type: SiteQuality
SIO_000300: -8.0e-3

QD
type: SiteQuality
SIO_000300: 1.066e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

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

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

Latino
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allele count: 4
allele frequency: 3.466204506065858e-4
allele num: 11540
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199220506670664e-4
allele num: 66710
num of homozygotes: 0

MQ
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SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

ReadPosRankSum
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QD
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VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 3.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

DP
type: SiteQuality
SIO_000300: 3.484186e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

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

East Asian
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allele frequency: 8.120649651972158e-4
allele num: 8620
num of homozygotes: 0

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

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

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

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

MQRankSum
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InbreedingCoeff
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QD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 3.635041802980734e-4
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

VQSLOD
type: SiteQuality
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.141e0

InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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InbreedingCoeff
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MQRankSum
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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SIO_000300: -1.114e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

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

GenotypeQuality
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variant carriers: 0

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

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

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

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

Other
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East Asian
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allele count: 0
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African
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FS
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.174e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.483506e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.26e-1

QD
type: SiteQuality
SIO_000300: 1.176e1

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

FS
type: SiteQuality
SIO_000300: 6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.55e-1

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

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

GenotypeQuality
all individuals: 1460
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2461
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45325
bin: 9.75e1
variant carriers: 9

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996821684507211e-5
allele num: 66702
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.423361201987156e-4
allele num: 16506
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.042e0

DP
type: SiteQuality
SIO_000300: 3.483853e6

FS
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

QD
type: SiteQuality
SIO_000300: 1.296e1