4-114280037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280037
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280037
    reference: chr 4
allele count: 2
allele frequency: 1.654725067430047e-5
allele num: 120866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1293C>T
  hgvsp: ENST00000505342.1:c.1293C>T(p.%3D)
  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.383-1942C>T
  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.10164C>T
  hgvsp: ENST00000264366.6:c.10164C>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.384-1942C>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.4427-1942C>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.10263C>T
  hgvsp: ENST00000357077.4:c.10263C>T(p.%3D)
  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.1955-1942C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1942C>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.4400-1942C>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.1431-1942C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8004
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala3421Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

4-114280038-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280038
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280038
    reference: chr 4
allele count: 1
allele frequency: 8.276364358664525e-6
allele num: 120826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1941G>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.4427-1941G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1294G>A
  hgvsp: ENSP00000422498.1:p.Glu432Lys
  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.10264G>A
  hgvsp: ENSP00000349588.4:p.Glu3422Lys
  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.383-1941G>A
  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.10165G>A
  hgvsp: ENSP00000264366.6:p.Glu3389Lys
  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.1955-1941G>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.384-1941G>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.4400-1941G>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.1431-1941G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8002
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu3422Lys
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

4-114280048-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280048
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280048
    reference: chr 4
allele count: 4
allele frequency: 3.31065534422539e-5
allele num: 120822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1931A>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.4427-1931A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1304A>G
  hgvsp: ENSP00000422498.1:p.Glu435Gly
  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.383-1931A>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.10274A>G
  hgvsp: ENSP00000349588.4:p.Glu3425Gly
  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.4400-1931A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1931A>G
  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.10175A>G
  hgvsp: ENSP00000264366.6:p.Glu3392Gly
  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.384-1931A>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.1431-1931A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17952
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9765
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu3425Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

4-114280057-CAGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280057
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280054
    reference: chr 4
allele count: 2
allele frequency: 1.655683963045134e-5
allele num: 120796
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.4427-1916_4427-1914delAAG
  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.384-1916_384-1914delAAG
  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.1955-1916_1955-1914delAAG
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1319_1321delAAG
  hgvsp: ENSP00000422498.1:p.Glu440del
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10289_10291delAAG
  hgvsp: ENSP00000349588.4:p.Glu3430del
  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.383-1916_383-1914delAAG
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.10190_10192delAAG
  hgvsp: ENSP00000264366.6:p.Glu3397del
  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.1431-1916_1431-1914delAAG
  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.4400-1916_4400-1914delAAG
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1916_536-1914delAAG
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8004
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Glu3430del
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: CAGA
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-114280063-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280063
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280063
    reference: chr 4
allele count: 19
allele frequency: 1.573446842340626e-4
allele num: 120754
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.1955-1916A>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.383-1916A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1916A>C
  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.10289A>C
  hgvsp: ENSP00000349588.4:p.Glu3430Ala
  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.1431-1916A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1319A>C
  hgvsp: ENSP00000422498.1:p.Glu440Ala
  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.4400-1916A>C
  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.10190A>C
  hgvsp: ENSP00000264366.6:p.Glu3397Ala
  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.4427-1916A>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.384-1916A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8412
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4989
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu3430Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
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: QD
site quality: ReadPosRankSum

4-114280095-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280095
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280095
    reference: chr 4
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.10222C>T
  hgvsp: ENSP00000264366.6:p.Arg3408Ter
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1884C>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.384-1884C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1351C>T
  hgvsp: ENSP00000422498.1:p.Arg451Ter
  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.4427-1884C>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.1955-1884C>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.1431-1884C>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.4400-1884C>T
  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.10321C>T
  hgvsp: ENSP00000349588.4:p.Arg3441Ter
  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.383-1884C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4110
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg3441Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS

4-114280096-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280096
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280096
    reference: chr 4
allele count: 8
allele frequency: 6.631189801230086e-5
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.383-1883G>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.1431-1883G>A
  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.10223G>A
  hgvsp: ENSP00000264366.6:p.Arg3408Gln
  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.10322G>A
  hgvsp: ENSP00000349588.4:p.Arg3441Gln
  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.1955-1883G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1352G>A
  hgvsp: ENSP00000422498.1:p.Arg451Gln
  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.384-1883G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1883G>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.4400-1883G>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.4427-1883G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4108
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg3441Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

4-114280097-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280097
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280097
    reference: chr 4
allele count: 2
allele frequency: 1.657742486282181e-5
allele num: 120646
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.10323A>T
  hgvsp: ENST00000357077.4:c.10323A>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.384-1882A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1882A>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.1431-1882A>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.383-1882A>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.1955-1882A>T
  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.10224A>T
  hgvsp: ENST00000264366.6:c.10224A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1353A>T
  hgvsp: ENST00000505342.1:c.1353A>T(p.%3D)
  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.4400-1882A>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.4427-1882A>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg3441Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

4-114280104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280104
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280104
    reference: chr 4
allele count: 2
allele frequency: 1.657989853102099e-5
allele num: 120628
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.1431-1875G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1360G>A
  hgvsp: ENSP00000422498.1:p.Val454Ile
  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.383-1875G>A
  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.10231G>A
  hgvsp: ENSP00000264366.6:p.Val3411Ile
  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.10330G>A
  hgvsp: ENSP00000349588.4:p.Val3444Ile
  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.4400-1875G>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.384-1875G>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.1955-1875G>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.4427-1875G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1875G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val3444Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

4-114280134-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280134
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280135
    reference: chr 4
allele count: 8
allele frequency: 6.64451827242525e-5
allele num: 120400
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1397dupG
  hgvsp: ENSP00000422498.1:p.Thr467HisfsTer8
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1838dupG
  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.10367dupG
  hgvsp: ENSP00000349588.4:p.Thr3457HisfsTer8
  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.384-1838dupG
  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.10268dupG
  hgvsp: ENSP00000264366.6:p.Thr3424HisfsTer8
  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.1431-1838dupG
  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.1955-1838dupG
  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.383-1838dupG
  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.4400-1838dupG
  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.4427-1838dupG
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9673
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr3457HisfsTer8
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

4-114280136-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280136
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280136
    reference: chr 4
allele count: 13
allele frequency: 1.078838174273859e-4
allele num: 120500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.10263G>T
  hgvsp: ENSP00000264366.6:p.Arg3421Ser
  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.10362G>T
  hgvsp: ENSP00000349588.4:p.Arg3454Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1392G>T
  hgvsp: ENSP00000422498.1:p.Arg464Ser
  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.383-1843G>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.4400-1843G>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1843G>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.1955-1843G>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.384-1843G>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.4427-1843G>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.1431-1843G>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg3454Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

4-114280136-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280136
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280136
    reference: chr 4
allele count: 21
allele frequency: 1.742738589211618e-4
allele num: 120500
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.10263G>C
  hgvsp: ENSP00000264366.6:p.Arg3421Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1843G>C
  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.10362G>C
  hgvsp: ENSP00000349588.4:p.Arg3454Ser
  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.1431-1843G>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.1955-1843G>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.383-1843G>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.4400-1843G>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.4427-1843G>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1392G>C
  hgvsp: ENSP00000422498.1:p.Arg464Ser
  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.384-1843G>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg3454Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

4-114280137-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280137
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280137
    reference: chr 4
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1842G>T
  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.10363G>T
  hgvsp: ENSP00000349588.4:p.Gly3455Trp
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1842G>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.384-1842G>T
  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.10264G>T
  hgvsp: ENSP00000264366.6:p.Gly3422Trp
  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.4427-1842G>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.4400-1842G>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1393G>T
  hgvsp: ENSP00000422498.1:p.Gly465Trp
  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.383-1842G>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.1431-1842G>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly3455Trp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

4-114280138-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280138
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280138
    reference: chr 4
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1394G>C
  hgvsp: ENSP00000422498.1:p.Gly465Ala
  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.1431-1841G>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.1955-1841G>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.4400-1841G>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1841G>C
  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.10364G>C
  hgvsp: ENSP00000349588.4:p.Gly3455Ala
  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.4427-1841G>C
  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.10265G>C
  hgvsp: ENSP00000264366.6:p.Gly3422Ala
  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.383-1841G>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.384-1841G>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly3455Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

4-114280141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280141
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280141
    reference: chr 4
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.383-1838G>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.384-1838G>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.4400-1838G>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.4427-1838G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1838G>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.1431-1838G>A
  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.10367G>A
  hgvsp: ENSP00000349588.4:p.Gly3456Asp
  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.10268G>A
  hgvsp: ENSP00000264366.6:p.Gly3423Asp
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1397G>A
  hgvsp: ENSP00000422498.1:p.Gly466Asp
  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.1955-1838G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly3456Asp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-114280145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280145
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280145
    reference: chr 4
allele count: 345
allele frequency: 2.86330815835339e-3
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10371G>A
  hgvsp: ENST00000357077.4:c.10371G>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.10272G>A
  hgvsp: ENST00000264366.6:c.10272G>A(p.%3D)
  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.383-1834G>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.384-1834G>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.1431-1834G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1834G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1401G>A
  hgvsp: ENST00000505342.1:c.1401G>A(p.%3D)
  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.1955-1834G>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.4400-1834G>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.4427-1834G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 15945
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 17953
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr3457Thr
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

4-114280149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280149
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280149
    reference: chr 4
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
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.4400-1830C>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.383-1830C>T
  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.10375C>T
  hgvsp: ENSP00000349588.4:p.Pro3459Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1405C>T
  hgvsp: ENSP00000422498.1:p.Pro469Ser
  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.4427-1830C>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.384-1830C>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.1955-1830C>T
  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.10276C>T
  hgvsp: ENSP00000264366.6:p.Pro3426Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1830C>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.1431-1830C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro3459Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/4-114280154-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280154
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280154
    reference: chr 4
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
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.384-1825A>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.383-1825A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1825A>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.4400-1825A>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.1431-1825A>C
  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.10380A>C
  hgvsp: ENST00000357077.4:c.10380A>C(p.%3D)
  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.4427-1825A>C
  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.10281A>C
  hgvsp: ENST00000264366.6:c.10281A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1410A>C
  hgvsp: ENST00000505342.1:c.1410A>C(p.%3D)
  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.1955-1825A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9730
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4982
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr3460Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-114280157-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280157
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280157
    reference: chr 4
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
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.4427-1822A>C
  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.10383A>C
  hgvsp: ENSP00000349588.4:p.Lys3461Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1822A>C
  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.10284A>C
  hgvsp: ENSP00000264366.6:p.Lys3428Asn
  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.1955-1822A>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.383-1822A>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.4400-1822A>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.1431-1822A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1413A>C
  hgvsp: ENSP00000422498.1:p.Lys471Asn
  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.384-1822A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys3461Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

4-114280157-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280157
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280157
    reference: chr 4
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10383A>G
  hgvsp: ENST00000357077.4:c.10383A>G(p.%3D)
  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.383-1822A>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.4427-1822A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1413A>G
  hgvsp: ENST00000505342.1:c.1413A>G(p.%3D)
  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.4400-1822A>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.384-1822A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1822A>G
  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.10284A>G
  hgvsp: ENST00000264366.6:c.10284A>G(p.%3D)
  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.1431-1822A>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.1955-1822A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25038
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys3461Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

4-114280166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280166
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280166
    reference: chr 4
allele count: 13
allele frequency: 1.078426492791134e-4
allele num: 120546
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10392G>A
  hgvsp: ENST00000357077.4:c.10392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1813G>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.383-1813G>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.4400-1813G>A
  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.10293G>A
  hgvsp: ENST00000264366.6:c.10293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1422G>A
  hgvsp: ENST00000505342.1:c.1422G>A(p.%3D)
  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.4427-1813G>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.1955-1813G>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.384-1813G>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.1431-1813G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8386
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3890
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9745
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys3464Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

4-114280169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280169
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280169
    reference: chr 4
allele count: 218
allele frequency: 1.808138281107443e-3
allele num: 120566
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.384-1810G>A
  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.10395G>A
  hgvsp: ENST00000357077.4:c.10395G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1810G>A
  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.10296G>A
  hgvsp: ENST00000264366.6:c.10296G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1425G>A
  hgvsp: ENST00000505342.1:c.1425G>A(p.%3D)
  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.1431-1810G>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.4400-1810G>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.1955-1810G>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.383-1810G>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.4427-1810G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 18040
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu3465Glu
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

4-114280197-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280197
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280197
    reference: chr 4
allele count: 2
allele frequency: 1.657302905251993e-5
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4427-1782A>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.10423A>G
  hgvsp: ENSP00000349588.4:p.Ile3475Val
  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.10324A>G
  hgvsp: ENSP00000264366.6:p.Ile3442Val
  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.383-1782A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1453A>G
  hgvsp: ENSP00000422498.1:p.Ile485Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1782A>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.1431-1782A>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.384-1782A>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.4400-1782A>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.1955-1782A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile3475Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

4-114280203-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280203
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280203
    reference: chr 4
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
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.1955-1776T>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.383-1776T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1776T>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.384-1776T>C
  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.10429T>C
  hgvsp: ENSP00000349588.4:p.Phe3477Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1459T>C
  hgvsp: ENSP00000422498.1:p.Phe487Leu
  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.4400-1776T>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.1431-1776T>C
  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.10330T>C
  hgvsp: ENSP00000264366.6:p.Phe3444Leu
  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.4427-1776T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe3477Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

4-114280220-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280220
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280220
    reference: chr 4
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
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.4400-1759T>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.1431-1759T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1476T>C
  hgvsp: ENST00000505342.1:c.1476T>C(p.%3D)
  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.4427-1759T>C
  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.10446T>C
  hgvsp: ENST00000357077.4:c.10446T>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.10347T>C
  hgvsp: ENST00000264366.6:c.10347T>C(p.%3D)
  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.383-1759T>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.384-1759T>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.1955-1759T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1759T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser3482Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

4-114280227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280227
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280227
    reference: chr 4
allele count: 2
allele frequency: 1.653876686954221e-5
allele num: 120928
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10453G>A
  hgvsp: ENSP00000349588.4:p.Ala3485Thr
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1752G>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.4400-1752G>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.384-1752G>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.1431-1752G>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.383-1752G>A
  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.10354G>A
  hgvsp: ENSP00000264366.6:p.Ala3452Thr
  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.1955-1752G>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.4427-1752G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1483G>A
  hgvsp: ENSP00000422498.1:p.Ala495Thr
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16073
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala3485Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/4-114280234-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280234
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280234
    reference: chr 4
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
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.383-1745A>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.1955-1745A>C
  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.10361A>C
  hgvsp: ENSP00000264366.6:p.Lys3454Thr
  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.4400-1745A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1745A>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.384-1745A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1490A>C
  hgvsp: ENSP00000422498.1:p.Lys497Thr
  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.1431-1745A>C
  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.10460A>C
  hgvsp: ENSP00000349588.4:p.Lys3487Thr
  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.4427-1745A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4084
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys3487Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-114280246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280246
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280246
    reference: chr 4
allele count: 18
allele frequency: 1.511766583239548e-4
allele num: 119066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1733G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1733G>A
  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.10373G>A
  hgvsp: ENSP00000264366.6:p.Arg3458Lys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1502G>A
  hgvsp: ENSP00000422498.1:p.Arg501Lys
  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.1431-1733G>A
  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.10472G>A
  hgvsp: ENSP00000349588.4:p.Arg3491Lys
  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.384-1733G>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.383-1733G>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.4400-1733G>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.4427-1733G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16141
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4907
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg3491Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

4-114280264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280264
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280264
    reference: chr 4
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.10391G>A
  hgvsp: ENSP00000264366.6:p.Arg3464Lys
  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.4400-1715G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1715G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1520G>A
  hgvsp: ENSP00000422498.1:p.Arg507Lys
  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.1955-1715G>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.1431-1715G>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.383-1715G>A
  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.10490G>A
  hgvsp: ENSP00000349588.4:p.Arg3497Lys
  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.4427-1715G>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.384-1715G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9864
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg3497Lys
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

4-114280277-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280277
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280277
    reference: chr 4
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
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.383-1702A>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.10503A>G
  hgvsp: ENSP00000349588.4:p.Ile3501Met
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1533A>G
  hgvsp: ENSP00000422498.1:p.Ile511Met
  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.10404A>G
  hgvsp: ENSP00000264366.6:p.Ile3468Met
  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.4427-1702A>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.1955-1702A>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.384-1702A>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.4400-1702A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1702A>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.1431-1702A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18304
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile3501Met
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-114280287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280287
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280287
    reference: chr 4
allele count: 2
allele frequency: 1.649538953862396e-5
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4427-1692G>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.1955-1692G>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.1431-1692G>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.383-1692G>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.4400-1692G>A
  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.10414G>A
  hgvsp: ENSP00000264366.6:p.Asp3472Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1543G>A
  hgvsp: ENSP00000422498.1:p.Asp515Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1692G>A
  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.10513G>A
  hgvsp: ENSP00000349588.4:p.Asp3505Asn
  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.384-1692G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18324
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp3505Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

4-114280293-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280293
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280293
    reference: chr 4
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
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.383-1686A>G
  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.10420A>G
  hgvsp: ENSP00000264366.6:p.Ser3474Gly
  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.4400-1686A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1549A>G
  hgvsp: ENSP00000422498.1:p.Ser517Gly
  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.384-1686A>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.1955-1686A>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.10519A>G
  hgvsp: ENSP00000349588.4:p.Ser3507Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1686A>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.4427-1686A>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.1431-1686A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8429
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser3507Gly
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

4-114280294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280294
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280294
    reference: chr 4
allele count: 2
allele frequency: 1.649158104787506e-5
allele num: 121274
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.384-1685G>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.1955-1685G>A
  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.10421G>A
  hgvsp: ENSP00000264366.6:p.Ser3474Asn
  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.10520G>A
  hgvsp: ENSP00000349588.4:p.Ser3507Asn
  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.383-1685G>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.4400-1685G>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.1431-1685G>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.4427-1685G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1550G>A
  hgvsp: ENSP00000422498.1:p.Ser517Asn
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1685G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16280
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4977
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser3507Asn
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

4-114280299-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280299
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280299
    reference: chr 4
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
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.383-1680A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1680A>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.1431-1680A>G
  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.10426A>G
  hgvsp: ENSP00000264366.6:p.Ser3476Gly
  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.4400-1680A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1555A>G
  hgvsp: ENSP00000422498.1:p.Ser519Gly
  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.10525A>G
  hgvsp: ENSP00000349588.4:p.Ser3509Gly
  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.384-1680A>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.4427-1680A>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.1955-1680A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4979
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7439
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser3509Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

4-114280305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280305
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280305
    reference: chr 4
allele count: 31
allele frequency: 2.556068601583114e-4
allele num: 121280
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.383-1674C>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.4400-1674C>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.384-1674C>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.10531C>T
  hgvsp: ENST00000357077.4:c.10531C>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.10432C>T
  hgvsp: ENST00000264366.6:c.10432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1674C>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.4427-1674C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1561C>T
  hgvsp: ENST00000505342.1:c.1561C>T(p.%3D)
  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.1955-1674C>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.1431-1674C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18304
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16269
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu3511Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

4-114280321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280321
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280321
    reference: chr 4
allele count: 9
allele frequency: 7.420966704596052e-5
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1658T>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.1431-1658T>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.4400-1658T>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.1955-1658T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1577T>C
  hgvsp: ENSP00000422498.1:p.Ile526Thr
  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.384-1658T>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.383-1658T>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.4427-1658T>C
  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.10448T>C
  hgvsp: ENSP00000264366.6:p.Ile3483Thr
  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.10547T>C
  hgvsp: ENSP00000349588.4:p.Ile3516Thr
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4978
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7438
  bin: 9.75e1
  variant carriers: 8
hgvs: p.Ile3516Thr
num of homozygotes: 1
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

4-114280329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280329
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280329
    reference: chr 4
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
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.10555C>T
  hgvsp: ENST00000357077.4:c.10555C>T(p.%3D)
  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.4400-1650C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1650C>T
  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.10456C>T
  hgvsp: ENST00000264366.6:c.10456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1585C>T
  hgvsp: ENST00000505342.1:c.1585C>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.384-1650C>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.383-1650C>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.4427-1650C>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.1431-1650C>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.1955-1650C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu3519Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

4-114280334-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280334
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280334
    reference: chr 4
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1645A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1590A>G
  hgvsp: ENST00000505342.1:c.1590A>G(p.%3D)
  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.4400-1645A>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.1431-1645A>G
  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.10461A>G
  hgvsp: ENST00000264366.6:c.10461A>G(p.%3D)
  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.4427-1645A>G
  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.10560A>G
  hgvsp: ENST00000357077.4:c.10560A>G(p.%3D)
  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.383-1645A>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.384-1645A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1645A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7435
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro3520Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

4-114280336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280336
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280336
    reference: chr 4
allele count: 4
allele frequency: 3.299023489047242e-5
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1643C>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.4400-1643C>T
  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.10562C>T
  hgvsp: ENSP00000349588.4:p.Pro3521Leu
  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.10463C>T
  hgvsp: ENSP00000264366.6:p.Pro3488Leu
  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.383-1643C>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.384-1643C>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.4427-1643C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1592C>T
  hgvsp: ENSP00000422498.1:p.Pro531Leu
  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.1955-1643C>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.1431-1643C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro3521Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/4-114280342-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280342
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280342
    reference: chr 4
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
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.4427-1637A>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.4400-1637A>C
  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.10568A>C
  hgvsp: ENSP00000349588.4:p.Glu3523Ala
  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.1431-1637A>C
  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.10469A>C
  hgvsp: ENSP00000264366.6:p.Glu3490Ala
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1598A>C
  hgvsp: ENSP00000422498.1:p.Glu533Ala
  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.384-1637A>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.383-1637A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1637A>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.1955-1637A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu3523Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

4-114280346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280346
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280346
    reference: chr 4
allele count: 2
allele frequency: 1.650246711883427e-5
allele num: 121194
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.384-1633C>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.4427-1633C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1633C>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.1955-1633C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1602C>T
  hgvsp: ENST00000505342.1:c.1602C>T(p.%3D)
  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.1431-1633C>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.4400-1633C>T
  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.10473C>T
  hgvsp: ENST00000264366.6:c.10473C>T(p.%3D)
  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.383-1633C>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.10572C>T
  hgvsp: ENST00000357077.4:c.10572C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9769
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr3524Thr
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: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-114280347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280347
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280347
    reference: chr 4
allele count: 7
allele frequency: 5.776149453741294e-5
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421067
  ensembl transcript: ENST00000506722
  gene symbol: ANK2
  hgvsc: ENST00000506722.1:c.4400-1632G>A
  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.10573G>A
  hgvsp: ENSP00000349588.4:p.Glu3525Lys
  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.1955-1632G>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.384-1632G>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.4427-1632G>A
  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.10474G>A
  hgvsp: ENSP00000264366.6:p.Glu3492Lys
  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.1431-1632G>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.383-1632G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1603G>A
  hgvsp: ENSP00000422498.1:p.Glu535Lys
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1632G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25611
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu3525Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114280352-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280352
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280352
    reference: chr 4
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
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.383-1627C>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.10578C>G
  hgvsp: ENSP00000349588.4:p.His3526Gln
  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.1955-1627C>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.1431-1627C>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.4400-1627C>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.384-1627C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1608C>G
  hgvsp: ENSP00000422498.1:p.His536Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1627C>G
  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.10479C>G
  hgvsp: ENSP00000264366.6:p.His3493Gln
  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.4427-1627C>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His3526Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

4-114280388-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280388
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280388
    reference: chr 4
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.383-1591T>A
  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.10515T>A
  hgvsp: ENST00000264366.6:c.10515T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1644T>A
  hgvsp: ENST00000505342.1:c.1644T>A(p.%3D)
  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.4400-1591T>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.1955-1591T>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.4427-1591T>A
  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.10614T>A
  hgvsp: ENST00000357077.4:c.10614T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1591T>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.384-1591T>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.1431-1591T>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile3538Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

4-114280388-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280388
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280388
    reference: chr 4
allele count: 2
allele frequency: 1.652237129072764e-5
allele num: 121048
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1644T>G
  hgvsp: ENSP00000422498.1:p.Ile548Met
  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.10614T>G
  hgvsp: ENSP00000349588.4:p.Ile3538Met
  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.4400-1591T>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.384-1591T>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.383-1591T>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1591T>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.1955-1591T>G
  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.10515T>G
  hgvsp: ENSP00000264366.6:p.Ile3505Met
  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.1431-1591T>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.4427-1591T>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile3538Met
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

4-114280393-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280393
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280393
    reference: chr 4
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
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.384-1586A>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.4400-1586A>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.4427-1586A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1649A>G
  hgvsp: ENSP00000422498.1:p.Asp550Gly
  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.383-1586A>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.1955-1586A>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.1431-1586A>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.10619A>G
  hgvsp: ENSP00000349588.4:p.Asp3540Gly
  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.10520A>G
  hgvsp: ENSP00000264366.6:p.Asp3507Gly
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1586A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2437
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp3540Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

4-114280401-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280401
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280401
    reference: chr 4
allele count: 3
allele frequency: 2.479912707072711e-5
allele num: 120972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4427-1578A>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.383-1578A>G
  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.10528A>G
  hgvsp: ENSP00000264366.6:p.Ile3510Val
  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.1955-1578A>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.1431-1578A>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.10627A>G
  hgvsp: ENSP00000349588.4:p.Ile3543Val
  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.384-1578A>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.4400-1578A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1657A>G
  hgvsp: ENSP00000422498.1:p.Ile553Val
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1578A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile3543Val
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

4-114280406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280406
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280406
    reference: chr 4
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000421023
  ensembl transcript: ENST00000510275
  gene symbol: ANK2
  hgvsc: ENST00000510275.2:c.383-1573G>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.4400-1573G>A
  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.10632G>A
  hgvsp: ENST00000357077.4:c.10632G>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.384-1573G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1573G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1662G>A
  hgvsp: ENST00000505342.1:c.1662G>A(p.%3D)
  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.1431-1573G>A
  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.10533G>A
  hgvsp: ENST00000264366.6:c.10533G>A(p.%3D)
  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.4427-1573G>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.1955-1573G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu3544Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

4-114280415-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280415
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280415
    reference: chr 4
allele count: 3
allele frequency: 2.482827112472068e-5
allele num: 120830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1564T>C
  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.10641T>C
  hgvsp: ENST00000357077.4:c.10641T>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.10542T>C
  hgvsp: ENST00000264366.6:c.10542T>C(p.%3D)
  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.4427-1564T>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.383-1564T>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.4400-1564T>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.1955-1564T>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.384-1564T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1671T>C
  hgvsp: ENST00000505342.1:c.1671T>C(p.%3D)
  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.1431-1564T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile3547Ile
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: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

4-114280420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280420
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280420
    reference: chr 4
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1559G>A
  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.10646G>A
  hgvsp: ENSP00000349588.4:p.Arg3549His
  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.4400-1559G>A
  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.10547G>A
  hgvsp: ENSP00000264366.6:p.Arg3516His
  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.383-1559G>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.1431-1559G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1676G>A
  hgvsp: ENSP00000422498.1:p.Arg559His
  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.1955-1559G>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.4427-1559G>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.384-1559G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg3549His
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

4-114280434-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280434
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280434
    reference: chr 4
allele count: 2
allele frequency: 1.657879903179814e-5
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.10561A>T
  hgvsp: ENSP00000264366.6:p.Asn3521Tyr
  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.10660A>T
  hgvsp: ENSP00000349588.4:p.Asn3554Tyr
  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.4427-1545A>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.1431-1545A>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.4400-1545A>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.384-1545A>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.1955-1545A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1690A>T
  hgvsp: ENSP00000422498.1:p.Asn564Tyr
  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.383-1545A>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1545A>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn3554Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

4-114280448-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280448
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280448
    reference: chr 4
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000264366
  ensembl transcript: ENST00000264366
  gene symbol: ANK2
  hgvsc: ENST00000264366.6:c.10575T>C
  hgvsp: ENST00000264366.6:c.10575T>C(p.%3D)
  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.1955-1531T>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.4400-1531T>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.384-1531T>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.4427-1531T>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.383-1531T>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.1431-1531T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1704T>C
  hgvsp: ENST00000505342.1:c.1704T>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.10674T>C
  hgvsp: ENST00000357077.4:c.10674T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1531T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4131
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His3558His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

4-114280471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280471
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280471
    reference: chr 4
allele count: 2
allele frequency: 1.671206778414693e-5
allele num: 119674
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.4427-1508C>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.10681+16C>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.383-1508C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1508C>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.4400-1508C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+16C>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.1955-1508C>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.384-1508C>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.1431-1508C>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.10582+16C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9667
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-114280485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280485
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280485
    reference: chr 4
allele count: 6
allele frequency: 5.059107236209717e-5
allele num: 118598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1494C>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.10681+30C>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.4400-1494C>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.384-1494C>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.1431-1494C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+30C>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.4427-1494C>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.383-1494C>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.10582+30C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1494C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15925
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16533
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4016
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-114280488-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280488
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280488
    reference: chr 4
allele count: 5
allele frequency: 4.226685602218164e-5
allele num: 118296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1491C>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.10582+33C>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.4400-1491C>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.4427-1491C>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.1431-1491C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1491C>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.384-1491C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+33C>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.383-1491C>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.10681+33C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16231
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-114280495-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280495
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280495
    reference: chr 4
allele count: 52
allele frequency: 4.423875314775743e-4
allele num: 117544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+40C>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.1431-1484C>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.1955-1484C>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.10582+40C>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.4427-1484C>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.384-1484C>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.4400-1484C>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1484C>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.10681+40C>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.383-1484C>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14614
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8694
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

4-114280495-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280495
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280495
    reference: chr 4
allele count: 1
allele frequency: 8.507452528414892e-6
allele num: 117544
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000426944
  ensembl transcript: ENST00000509550
  gene symbol: ANK2
  hgvsc: ENST00000509550.1:c.1955-1484C>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.4400-1484C>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.10681+40C>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.4427-1484C>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.1431-1484C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1484C>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+40C>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.383-1484C>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.384-1484C>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.10582+40C>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7463
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

4-114280497-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280497
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280497
    reference: chr 4
allele count: 1
allele frequency: 8.527039241434588e-6
allele num: 117274
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.1955-1482T>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.1431-1482T>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.10582+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.10681+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.383-1482T>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.384-1482T>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.4400-1482T>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.4427-1482T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1482T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+42T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14254
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/4-114280499-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280499
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280499
    reference: chr 4
allele count: 163
allele frequency: 1.39197267292912e-3
allele num: 117100
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10681+44A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+44A>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.4400-1480A>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1480A>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.1431-1480A>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.384-1480A>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.4427-1480A>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.10582+44A>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.383-1480A>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.1955-1480A>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 13787
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13479
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3823
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

4-114280506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280506
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280506
    reference: chr 4
allele count: 1
allele frequency: 8.597565169543985e-6
allele num: 116312
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10681+51T>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.4427-1473T>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.383-1473T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+51T>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.384-1473T>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.4400-1473T>C
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1473T>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.1955-1473T>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.1431-1473T>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.10582+51T>C
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

4-114280507-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114280507
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114280507
    reference: chr 4
allele count: 48
allele frequency: 4.125696211235646e-4
allele num: 116344
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.1431-1472A>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.384-1472A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-1472A>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.10582+52A>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.4427-1472A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1711+52A>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.4400-1472A>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.1955-1472A>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.10681+52A>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.383-1472A>G
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13526
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11840
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

4-114281931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281931
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281931
    reference: chr 4
allele count: 1
allele frequency: 1.119595154392172e-5
allele num: 89318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-48C>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.4400-48C>T
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1712-48C>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.383-48C>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.1431-48C>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.10583-48C>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.384-48C>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.1955-48C>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.4427-48C>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.10682-48C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2610
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114281942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281942
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281942
    reference: chr 4
allele count: 2
allele frequency: 2.202885780372288e-5
allele num: 90790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4427-37G>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.1431-37G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.536-37G>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.384-37G>A
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1712-37G>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.4400-37G>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.383-37G>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.1955-37G>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.10682-37G>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.10583-37G>A
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17961
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7772
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

4-114281981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281981
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281981
    reference: chr 4
allele count: 2
allele frequency: 1.834088366377492e-5
allele num: 109046
alternate allele: T
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.386C>T
  hgvsp: ENSP00000426994.1:p.Pro130Ser
  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.4429C>T
  hgvsp: ENSP00000378044.3:p.Pro1477Ser
  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.4402C>T
  hgvsp: ENSP00000421067.1:p.Pro1468Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1714C>T
  hgvsp: ENSP00000422498.1:p.Pro572Ser
  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.10585C>T
  hgvsp: ENSP00000264366.6:p.Pro3529Ser
  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.1433C>T
  hgvsp: ENSP00000422853.1:p.Pro479Ser
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.538C>T
  variant of: http://identifiers.org/hgnc/493
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.10684C>T
  hgvsp: ENSP00000349588.4:p.Pro3562Ser
  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.385C>T
  hgvsp: ENSP00000421023.2:p.Pro129Ser
  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.1957C>T
  hgvsp: ENSP00000426944.1:p.Pro653Ser
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34336
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro3562Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/4-114281982-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281982
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281982
    reference: chr 4
allele count: 1
allele frequency: 9.139932364500503e-6
allele num: 109410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000349588
  ensembl transcript: ENST00000357077
  gene symbol: ANK2
  hgvsc: ENST00000357077.4:c.10685C>A
  hgvsp: ENSP00000349588.4:p.Pro3562Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1715C>A
  hgvsp: ENSP00000422498.1:p.Pro572Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.539C>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.4430C>A
  hgvsp: ENSP00000378044.3:p.Pro1477Gln
  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.386C>A
  hgvsp: ENSP00000421023.2:p.Pro129Gln
  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.1434C>A
  hgvsp: ENSP00000422853.1:p.Pro479Gln
  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.1958C>A
  hgvsp: ENSP00000426944.1:p.Pro653Gln
  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.4403C>A
  hgvsp: ENSP00000421067.1:p.Pro1468Gln
  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.10586C>A
  hgvsp: ENSP00000264366.6:p.Pro3529Gln
  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.387C>A
  hgvsp: ENSP00000426994.1:p.Pro130Gln
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro3562Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

4-114281982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281982
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281982
    reference: chr 4
allele count: 2
allele frequency: 1.827986472900101e-5
allele num: 109410
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.1958C>T
  hgvsp: ENSP00000426944.1:p.Pro653Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.539C>T
  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.386C>T
  hgvsp: ENSP00000421023.2:p.Pro129Leu
  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.10685C>T
  hgvsp: ENSP00000349588.4:p.Pro3562Leu
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1715C>T
  hgvsp: ENSP00000422498.1:p.Pro572Leu
  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.10586C>T
  hgvsp: ENSP00000264366.6:p.Pro3529Leu
  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.4403C>T
  hgvsp: ENSP00000421067.1:p.Pro1468Leu
  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.1434C>T
  hgvsp: ENSP00000422853.1:p.Pro479Leu
  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.387C>T
  hgvsp: ENSP00000426994.1:p.Pro130Leu
  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.4430C>T
  hgvsp: ENSP00000378044.3:p.Pro1477Leu
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34568
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro3562Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

4-114281983-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281983
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281983
    reference: chr 4
allele count: 1
allele frequency: 9.099677871403353e-6
allele num: 109894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.540A>G
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1716A>G
  hgvsp: ENST00000505342.1:c.1716A>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.1435A>G
  hgvsp: ENST00000514960.1:c.1435A>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.1959A>G
  hgvsp: ENST00000509550.1:c.1959A>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.4404A>G
  hgvsp: ENST00000506722.1:c.4404A>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.4431A>G
  hgvsp: ENST00000394537.3:c.4431A>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.10587A>G
  hgvsp: ENST00000264366.6:c.10587A>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.388A>G
  hgvsp: ENST00000504415.1:c.388A>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.387A>G
  hgvsp: ENST00000510275.2:c.387A>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.10686A>G
  hgvsp: ENST00000357077.4:c.10686A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro3562Pro
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

4-114281999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114281999
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114281999
    reference: chr 4
allele count: 19
allele frequency: 1.68129689933456e-4
allele num: 113008
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.1975C>T
  hgvsp: ENSP00000426944.1:p.Arg659Trp
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1732C>T
  hgvsp: ENSP00000422498.1:p.Arg578Trp
  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.10603C>T
  hgvsp: ENSP00000264366.6:p.Arg3535Trp
  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.404C>T
  hgvsp: ENSP00000426994.1:p.Arg136Trp
  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.10702C>T
  hgvsp: ENSP00000349588.4:p.Arg3568Trp
  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.4420C>T
  hgvsp: ENSP00000421067.1:p.Arg1474Trp
  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.1451C>T
  hgvsp: ENSP00000422853.1:p.Arg485Trp
  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.4447C>T
  hgvsp: ENSP00000378044.3:p.Arg1483Trp
  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.403C>T
  hgvsp: ENSP00000421023.2:p.Arg135Trp
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.556C>T
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35791
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg3568Trp
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-114282000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114282000
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114282000
    reference: chr 4
allele count: 5
allele frequency: 4.42008486562942e-5
allele num: 113120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000378044
  ensembl transcript: ENST00000394537
  gene symbol: ANK2
  hgvsc: ENST00000394537.3:c.4448G>A
  hgvsp: ENSP00000378044.3:p.Arg1483Gln
  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.4421G>A
  hgvsp: ENSP00000421067.1:p.Arg1474Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145362
  ensembl transcript: ENST00000508007
  gene symbol: ANK2
  hgvsc: ENST00000508007.1:n.557G>A
  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.405G>A
  hgvsp: ENSP00000426994.1:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145362
  ensembl protein: ENSP00000422498
  ensembl transcript: ENST00000505342
  gene symbol: ANK2
  hgvsc: ENST00000505342.1:c.1733G>A
  hgvsp: ENSP00000422498.1:p.Arg578Gln
  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.404G>A
  hgvsp: ENSP00000421023.2:p.Arg135Gln
  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.1452G>A
  hgvsp: ENSP00000422853.1:p.Arg485Gln
  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.1976G>A
  hgvsp: ENSP00000426944.1:p.Arg659Gln
  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.10604G>A
  hgvsp: ENSP00000264366.6:p.Arg3535Gln
  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.10703G>A
  hgvsp: ENSP00000349588.4:p.Arg3568Gln
  variant of: http://identifiers.org/hgnc/493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35744
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Arg3568Gln
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 4115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4991
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3888
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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: 904
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 2.069743e6

FS
type: SiteQuality
SIO_000300: 3.378e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.23e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

GenotypeQuality
all individuals: 2412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24938
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4991
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 2.069523e6

VQSLOD
type: SiteQuality
SIO_000300: -2.601e0

QD
type: SiteQuality
SIO_000300: 1.359e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.7462e1

MQ
type: SiteQuality
SIO_000300: 5.838e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

GenotypeQuality
all individuals: 4112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3887
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4996
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8011
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24960
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.424242424242424e-4
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.14e-1

FS
type: SiteQuality
SIO_000300: 9.57e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.33e-1

DP
type: SiteQuality
SIO_000300: 2.068445e6

QD
type: SiteQuality
SIO_000300: 1.443e1

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

GenotypeQuality
all individuals: 289
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24952
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3884
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4990
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

MQ
type: SiteQuality
SIO_000300: 5.819e1

FS
type: SiteQuality
SIO_000300: 6.13e-1

DP
type: SiteQuality
SIO_000300: 2.06819e6

QD
type: SiteQuality
SIO_000300: 1.795e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 24842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8018
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 9736
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1765
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3887
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 18
allele frequency: 1.810136765888978e-3
allele num: 9944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
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: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
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: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e0

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

DP
type: SiteQuality
SIO_000300: 2.068505e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 3.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.32e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3890
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8000
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9880
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

DP
type: SiteQuality
SIO_000300: 2.064544e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

FS
type: SiteQuality
SIO_000300: 8.323e0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24905
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8003
bin: 9.75e1
variant carriers: 8

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

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.012555690562981e-4
allele num: 9876
num of homozygotes: 0

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

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

East Asian
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allele count: 7
allele frequency: 8.145217593670003e-4
allele num: 8594
num of homozygotes: 0

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

QD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -8.0e-4

ReadPosRankSum
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SIO_000300: 7.15e-1

ClippingRankSum
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SIO_000300: -1.36e-1

DP
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SIO_000300: 2.064663e6

VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

BaseQRankSum
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SIO_000300: -2.335e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 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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MQ
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SIO_000300: 6.0e1

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

QD
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VQSLOD
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SIO_000300: 9.08e-1

BaseQRankSum
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SIO_000300: 3.65e0

MQRankSum
type: SiteQuality
SIO_000300: 7.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.84e-1

DP
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SIO_000300: 2.064111e6

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

Latino
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allele frequency: 0.0e0
allele num: 11540
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Other
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allele frequency: 0.0e0
allele num: 904
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 2
allele frequency: 2.026753141467369e-4
allele num: 9868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66592
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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FS
type: SiteQuality
SIO_000300: 3.8e0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

BaseQRankSum
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SIO_000300: -4.451e0

ClippingRankSum
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SIO_000300: 4.86e-1

DP
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QD
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MQRankSum
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MQ
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SIO_000300: 5.964e1

VQSLOD
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SIO_000300: 1.37e0

ReadPosRankSum
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SIO_000300: -6.879999999999999e-1

GenotypeQuality
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variant carriers: 2

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

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

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

Latino
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allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.032520325203252e-4
allele num: 9840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.526719855486979e-5
allele num: 66430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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QD
type: SiteQuality
SIO_000300: 3.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 2.067113e6

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

FS
type: SiteQuality
SIO_000300: 8.05e-1

ReadPosRankSum
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SIO_000300: -2.16e-1

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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South 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 count: 11
allele frequency: 1.116524563540398e-3
allele num: 9852
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007337904486948e-5
allele num: 66504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 2.061433e6

VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
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SIO_000300: 3.86e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

African
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allele count: 6
allele frequency: 6.090133982947625e-4
allele num: 9852
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.007337904486948e-5
allele num: 66504
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East Asian
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allele num: 8594
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South Asian
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allele frequency: 4.240882103477523e-4
allele num: 16506
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Other
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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SIO_000300: 1.6e-3

BaseQRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Latino
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allele frequency: 8.671522719389525e-5
allele num: 11532
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South Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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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
all individuals: 106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 1749
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
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: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.468e0

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.169e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.283e0

QD
type: SiteQuality
SIO_000300: 1.05e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.059561e6

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.5e0
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GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 9.25e1
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GenotypeQuality
all individuals: 110
bin: 3.75e1
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GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 344

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 7.100831811726517e-4
allele num: 9858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 297
allele frequency: 4.465493910690121e-3
allele num: 66510
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.38864780420066e-3
allele num: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.513775355737209e-3
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.48073661255149e-4
allele num: 16508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.062335e6

FS
type: SiteQuality
SIO_000300: 5.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7753
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1748
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
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: 6606
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.486e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

DP
type: SiteQuality
SIO_000300: 2.051661e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
all individuals: 150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 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: 902
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 1.344e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 2.05166e6

FS
type: SiteQuality
SIO_000300: 8.143000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

GenotypeQuality
all individuals: 25038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 7753
bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
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GenotypeQuality
all individuals: 9734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3891
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

FS
type: SiteQuality
SIO_000300: 1.965e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e0

MQRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.454e0

QD
type: SiteQuality
SIO_000300: 1.501e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.051902e6

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-1

GenotypeQuality
all individuals: 7753
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 95
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GenotypeQuality
all individuals: 19
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4079
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9876
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.965e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.051902e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e0

MQRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.454e0

QD
type: SiteQuality
SIO_000300: 1.501e1

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7760
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 13
allele frequency: 1.513387660069849e-3
allele num: 8590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

DP
type: SiteQuality
SIO_000300: 2.052553e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.375e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.236e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

FS
type: SiteQuality
SIO_000300: 2.637e0

GenotypeQuality
all individuals: 25009
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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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: 7885
bin: 9.75e1
variant carriers: 216

GenotypeQuality
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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: 4053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 8.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 211
allele frequency: 3.171596921596922e-3
allele num: 66528
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
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: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.061830672863204e-4
allele num: 9898
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.293e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

QD
type: SiteQuality
SIO_000300: 1.376e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.93e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.057854e6

GenotypeQuality
all individuals: 4066
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 2408
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GenotypeQuality
all individuals: 402
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GenotypeQuality
all individuals: 77
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GenotypeQuality
all individuals: 13
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 2
allele frequency: 2.326122354035822e-4
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
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: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 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

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

DP
type: SiteQuality
SIO_000300: 2.052708e6

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.53e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.374e1

MQRankSum
type: SiteQuality
SIO_000300: 8.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 5.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

Latino
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 2.05322e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -1.276e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
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: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.1389e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.609e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e0

QD
type: SiteQuality
SIO_000300: 1.769e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 2.054758e6

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4080
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.978239366963402e-4
allele num: 10110
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

FS
type: SiteQuality
SIO_000300: 3.044e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 2.055581e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.972e0

QD
type: SiteQuality
SIO_000300: 1.382e1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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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: 35
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.512e1

DP
type: SiteQuality
SIO_000300: 2.055546e6

VQSLOD
type: SiteQuality
SIO_000300: 6.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.44e0

FS
type: SiteQuality
SIO_000300: 2.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-1

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 9627
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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: 8.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.068604402650139e-4
allele num: 65506
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.45179584120983e-4
allele num: 6348
num of homozygotes: 0

African
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allele count: 5
allele frequency: 5.140859551717047e-4
allele num: 9726
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.159e2

ClippingRankSum
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SIO_000300: 2.27e0

FS
type: SiteQuality
SIO_000300: 1.56282e2

QD
type: SiteQuality
SIO_000300: 5.4e-1

DP
type: SiteQuality
SIO_000300: 2.05871e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.451e0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e0

MQ
type: SiteQuality
SIO_000300: 5.838e1

GenotypeQuality
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variant carriers: 0

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

African
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: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.743e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.303e0

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.663e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

FS
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 2.036069e6

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.5e1

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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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7441
bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.23e-1

DP
type: SiteQuality
SIO_000300: 2.03635e6

VQSLOD
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 3.136e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.413e1

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 7.068e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.83e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.622000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

DP
type: SiteQuality
SIO_000300: 2.036296e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.334e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.04e-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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variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 2.036363e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

FS
type: SiteQuality
SIO_000300: 2.326e0

QD
type: SiteQuality
SIO_000300: 1.412e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -1.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

DP
type: SiteQuality
SIO_000300: 2.036363e6

FS
type: SiteQuality
SIO_000300: 1.038e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.53e-1

QD
type: SiteQuality
SIO_000300: 1.666e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 31

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 4070
bin: 7.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 4
allele frequency: 3.459609064175748e-4
allele num: 11562
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.899103206262559e-4
allele num: 66682
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 2.038765e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.32e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.012e0

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.63821892393321e-4
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 11564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.029935765361775e-4
allele num: 16502
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.789e0

FS
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 2.035594e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 1.638e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 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: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 2
allele frequency: 3.000030000300003e-5
allele num: 66666
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.67e-1

QD
type: SiteQuality
SIO_000300: 1.234e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.895e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

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

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

Latino
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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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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.000420029402058e-5
allele num: 66662
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

ClippingRankSum
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SIO_000300: -6.68e-1

FS
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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SIO_000300: 5.952e1

BaseQRankSum
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SIO_000300: -3.172e0

QD
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SIO_000300: 1.252e1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8630
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10382
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.67e-1

FS
type: SiteQuality
SIO_000300: 7.93e-1

VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
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allele frequency: 1.500555205426008e-5
allele num: 66642
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: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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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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bin: 9.75e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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South Asian
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allele count: 7
allele frequency: 4.251184258472003e-4
allele num: 16466
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

FS
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SIO_000300: 1.095e0

DP
type: SiteQuality
SIO_000300: 2.033658e6

MQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
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SIO_000300: 5.4e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
type: SiteQuality
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DP
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SIO_000300: 2.03274e6

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502403846153846e-5
allele num: 66560
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66560
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South Asian
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East Asian
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FS
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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ClippingRankSum
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FS
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MQ
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MQRankSum
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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.484320557491289e-4
allele num: 8610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

European (Finnish)
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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
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.023e0

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

QD
type: SiteQuality
SIO_000300: 1.474e1

DP
type: SiteQuality
SIO_000300: 2.0327e6

VQSLOD
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 1.363e0

MQ
type: SiteQuality
SIO_000300: 5.921e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (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: 66486
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.742790335151988e-5
allele num: 10264
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.222e1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 2.031642e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.429999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.184e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 2.603e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

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: 3

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009147809340395e-5
allele num: 66464
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: 9.778994719342852e-5
allele num: 10226
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.030812e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.748e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.12e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2439
bin: 9.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.577e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.338e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.154e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 2.030251e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.05e-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
all individuals: 51
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GenotypeQuality
all individuals: 5109
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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: 2
allele frequency: 3.014227152158187e-5
allele num: 66352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

FS
type: SiteQuality
SIO_000300: 1.218e0

DP
type: SiteQuality
SIO_000300: 2.027439e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.397e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.287e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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MQRankSum
type: SiteQuality
SIO_000300: -4.33e-1

DP
type: SiteQuality
SIO_000300: 2.023038e6

MQ
type: SiteQuality
SIO_000300: 5.896e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.645e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

FS
type: SiteQuality
SIO_000300: 2.077e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

ReadPosRankSum
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SIO_000300: 1.3e0

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: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9836
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036744609778318e-5
allele num: 65860
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 5.43e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 9.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 2.00814e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7423
bin: 9.75e1
variant carriers: 6

Latino
type: Population
allele count: 6
allele frequency: 5.247507433968865e-4
allele num: 11434
num of homozygotes: 0

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

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

African
type: Population
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: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65236
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.976161e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
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SIO_000300: -3.424e0

FS
type: SiteQuality
SIO_000300: 1.091e0

QD
type: SiteQuality
SIO_000300: 1.376e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeQuality
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bin: 1.75e1
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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3899
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.075314450902605e-5
allele num: 65034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.824373631719776e-4
allele num: 16444
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.966379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

FS
type: SiteQuality
SIO_000300: 5.926e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.428e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 52

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

South Asian
type: Population
allele count: 51
allele frequency: 3.10445580715851e-3
allele num: 16428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64586
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.785802143735723e-5
allele num: 11382
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

FS
type: SiteQuality
SIO_000300: 7.35e-1

DP
type: SiteQuality
SIO_000300: 1.923586e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

QD
type: SiteQuality
SIO_000300: 1.25e1

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
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179245283018868e-4
allele num: 8480
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64586
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e0

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

DP
type: SiteQuality
SIO_000300: 1.923586e6

FS
type: SiteQuality
SIO_000300: 7.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

QD
type: SiteQuality
SIO_000300: 1.25e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

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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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64420
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: 6.091617933723197e-5
allele num: 16416
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.905399e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

FS
type: SiteQuality
SIO_000300: 3.174e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

QD
type: SiteQuality
SIO_000300: 1.346e1

MQRankSum
type: SiteQuality
SIO_000300: -2.18e-1

GenotypeQuality
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bin: 7.5e0
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 163

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 150
allele frequency: 1.641137855579869e-2
allele num: 9140
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.285412262156448e-4
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.088274618326545e-4
allele num: 64322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

QD
type: SiteQuality
SIO_000300: 1.577e1

VQSLOD
type: SiteQuality
SIO_000300: 6.67e0

DP
type: SiteQuality
SIO_000300: 1.894572e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 5.75e1
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: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564994209521425e-5
allele num: 63898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.698e0

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.869449e6

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.671e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

MQ
type: SiteQuality
SIO_000300: 5.824e1

QD
type: SiteQuality
SIO_000300: 1.86e1

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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.355242566510173e-4
allele num: 63900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.844861135680169e-5
allele num: 11306
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.24e0

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: 49130
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.086689309396733e-5
allele num: 12366
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Latino
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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: 6112
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
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MQ
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MQRankSum
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QD
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.000720259293346e-5
allele num: 49982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.992327365728901e-5
allele num: 12512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

DP
type: SiteQuality
SIO_000300: 1.658808e6

QD
type: SiteQuality
SIO_000300: 1.183e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

GenotypeDepth
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 528
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
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
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.40548137737175e-4
allele num: 14230
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.977624e6

VQSLOD
type: SiteQuality
SIO_000300: 7.15e-1

FS
type: SiteQuality
SIO_000300: 2.755e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.897e0

QD
type: SiteQuality
SIO_000300: 1.051e1

GenotypeQuality
all individuals: 36805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.649130908011478e-5
allele num: 60638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

FS
type: SiteQuality
SIO_000300: 9.151e0

VQSLOD
type: SiteQuality
SIO_000300: -1.508e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

QD
type: SiteQuality
SIO_000300: 8.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

DP
type: SiteQuality
SIO_000300: 1.983062e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6225
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1842
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9897
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.298261816022956e-5
allele num: 60638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

DP
type: SiteQuality
SIO_000300: 1.983062e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 9.151e0

QD
type: SiteQuality
SIO_000300: 8.58e0

VQSLOD
type: SiteQuality
SIO_000300: -1.508e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeQuality
all individuals: 966
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6052
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 428
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GenotypeQuality
all individuals: 145
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 481
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GenotypeQuality
all individuals: 458
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variant carriers: 0

GenotypeQuality
all individuals: 278
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GenotypeQuality
all individuals: 457
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GenotypeQuality
all individuals: 9894
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variant carriers: 1

GenotypeQuality
all individuals: 37285
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GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
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GenotypeQuality
all individuals: 341
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GenotypeQuality
all individuals: 242
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GenotypeQuality
all individuals: 318
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9394
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.980315510261064e-5
allele num: 14326
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.279e0

QD
type: SiteQuality
SIO_000300: 1.156e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.064e0

DP
type: SiteQuality
SIO_000300: 1.987197e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.97e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
all individuals: 48
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 484
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GenotypeQuality
all individuals: 342
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.071251035625518e-4
allele num: 9656
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.877581674802854e-4
allele num: 10652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.395859953999489e-4
allele num: 62608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6156
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

FS
type: SiteQuality
SIO_000300: 2.551e0

DP
type: SiteQuality
SIO_000300: 2.027746e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.019e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1