12-974499-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 974499
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 974499
    reference: chr 12
allele count: 1
allele frequency: 8.210180623973728e-5
allele num: 12180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.97+3063G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2139+3063G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2363G>A
  hgvsp: ENSP00000433548.2:p.Arg788His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+3063G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-2533G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+3063G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.918+3063G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2139+3063G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg788His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-974515-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 974515
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 974515
    reference: chr 12
allele count: 1
allele frequency: 8.315316813570597e-5
allele num: 12026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.97+3079C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2139+3079C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-2517C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2139+3079C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.918+3079C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2379C>T
  hgvsp: ENST00000530271.2:c.2379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+3079C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+3079C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser793Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

12-974516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 974516
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 974516
    reference: chr 12
allele count: 1
allele frequency: 8.320852055250458e-5
allele num: 12018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+3080C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.97+3080C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-2516C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2139+3080C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2380C>T
  hgvsp: ENSP00000433548.2:p.Leu794Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+3080C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.918+3080C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2139+3080C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4059
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu794Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

12-974544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 974544
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 974544
    reference: chr 12
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+3108A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2139+3108A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2139+3108A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.918+3108A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.97+3108A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-2488A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+3108A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2394+14A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

12-974559-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 974559
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 974559
    reference: chr 12
allele count: 16
allele frequency: 1.424247819120527e-3
allele num: 11234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2394+29A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-2473A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+3123A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+3123A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2139+3123A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.918+3123A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2139+3123A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.97+3123A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

12-976946-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976946
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976946
    reference: chr 12
allele count: 3
allele frequency: 3.875968992248062e-5
allele num: 77400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-86G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3485G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3485G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-86G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5510G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5510G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3485G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3485G>T
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18674
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19792
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

12-976949-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976949
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976949
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 77572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-83A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3482A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5513A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3482A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3482A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5513A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-83A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3482A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18658
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5694
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-976950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976950
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976950
    reference: chr 12
allele count: 1
allele frequency: 1.291789386658399e-5
allele num: 77412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-82C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3481C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5514C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3481C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-82C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3481C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5514C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3481C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13846
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/12-976952-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976952
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976952
    reference: chr 12
allele count: 1
allele frequency: 1.290255986787779e-5
allele num: 77504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3479C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-80C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-80C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5516C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3479C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5516C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3479C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3479C>A
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7654
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5682
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8610
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

12-976958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976958
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976958
    reference: chr 12
allele count: 4
allele frequency: 5.102691669855849e-5
allele num: 78390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3473T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5522T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3473T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5522T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3473T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-74T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-74T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3473T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19569
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18790
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 5798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16059
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

12-976977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976977
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976977
    reference: chr 12
allele count: 1
allele frequency: 1.219482451647521e-5
allele num: 82002
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3454G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-55G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.-19G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3454G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5541G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-55G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5541G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3454G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3454G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5143
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

12-976996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976996
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976996
    reference: chr 12
allele count: 2
allele frequency: 2.231943576466387e-5
allele num: 89608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3435A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5560A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3435A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.1A>G
  hgvsp: ENSP00000460651.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-36A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5560A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3435A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-36A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3435A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5013
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

12-976996-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976996
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976995
    reference: chr 12
allele count: 1
allele frequency: 1.115971788233193e-5
allele num: 89608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.2delT
  hgvsp: ENSP00000460651.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3434delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5561delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-35delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3434delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3434delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3434delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-35delT
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5561delT
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5013
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: AT
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

12-976998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 976998
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 976998
    reference: chr 12
allele count: 3
allele frequency: 3.317263036843735e-5
allele num: 90436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-34G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3433G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.3G>A
  hgvsp: ENSP00000460651.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3433G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5562G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3433G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5562G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3433G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-34G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

12-977006-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977006
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977007
    reference: chr 12
allele count: 1
allele frequency: 1.059142518217251e-5
allele num: 94416
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.12dupA
  hgvsp: ENSP00000460651.1:p.Leu5ThrfsTer34
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5571dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5571dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3424dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-25dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3424dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3424dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-25dupA
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3424dupA
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 24297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu5ThrfsTer34
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

12-977009-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977009
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977009
    reference: chr 12
allele count: 1
allele frequency: 1.039436209799805e-5
allele num: 96206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3422T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3422T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.14T>C
  hgvsp: ENSP00000460651.1:p.Leu5Pro
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3422T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5573T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3422T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-23T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5573T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-23T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7977
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3855
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu5Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-977017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977017
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977017
    reference: chr 12
allele count: 3
allele frequency: 2.960565270595666e-5
allele num: 101332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3414T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-15T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-15T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5581T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3414T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.22T>C
  hgvsp: ENSP00000460651.1:p.Phe8Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3414T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3414T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5581T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2939
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe8Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

12-977020-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977020
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977020
    reference: chr 12
allele count: 1
allele frequency: 9.670244657189828e-6
allele num: 103410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-12A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3411A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.25A>G
  hgvsp: ENSP00000460651.1:p.Met9Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-12A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3411A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3411A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5584A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3411A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5584A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met9Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

12-977031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977031
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977031
    reference: chr 12
allele count: 1
allele frequency: 9.073422131891263e-6
allele num: 110212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5595G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3400G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5595G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3400G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.36G>A
  hgvsp: ENST00000574564.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3400G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3400G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2140-1G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2395-1G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36282
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 2.75e1
  variant carriers: 0
hgvs: c.2140-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

12-977040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977040
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977040
    reference: chr 12
allele count: 1
allele frequency: 8.733319360022357e-6
allele num: 114504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3391C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2148C>T
  hgvsp: ENST00000537687.1:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5604C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3391C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2403C>T
  hgvsp: ENST00000530271.2:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5604C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.45C>T
  hgvsp: ENST00000574564.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3391C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3391C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser716Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-977041-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977041
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977041
    reference: chr 12
allele count: 2
allele frequency: 1.739614501426484e-5
allele num: 114968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2149A>G
  hgvsp: ENSP00000444465.1:p.Met717Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.46A>G
  hgvsp: ENSP00000460651.1:p.Met16Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3390A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3390A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2404A>G
  hgvsp: ENSP00000433548.2:p.Met802Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3390A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3390A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5605A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5605A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12353
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met717Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

12-977042-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977042
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977042
    reference: chr 12
allele count: 1
allele frequency: 8.680555555555556e-6
allele num: 115200
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3389T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2405T>G
  hgvsp: ENSP00000433548.2:p.Met802Arg
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3389T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5606T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.47T>G
  hgvsp: ENSP00000460651.1:p.Met16Arg
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3389T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2150T>G
  hgvsp: ENSP00000444465.1:p.Met717Arg
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3389T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5606T>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38832
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46984
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met717Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

12-977045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977045
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977045
    reference: chr 12
allele count: 2
allele frequency: 1.727921483247801e-5
allele num: 115746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5609C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2408C>T
  hgvsp: ENSP00000433548.2:p.Ala803Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2153C>T
  hgvsp: ENSP00000444465.1:p.Ala718Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3386C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3386C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3386C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3386C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.50C>T
  hgvsp: ENSP00000460651.1:p.Ala17Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5609C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13012
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala718Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

12-977046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977046
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977046
    reference: chr 12
allele count: 2
allele frequency: 1.722385848877866e-5
allele num: 116118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2409G>A
  hgvsp: ENST00000530271.2:c.2409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3385G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2154G>A
  hgvsp: ENST00000537687.1:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5610G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3385G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.51G>A
  hgvsp: ENST00000574564.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5610G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3385G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3385G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13448
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala718Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-977051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977051
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977051
    reference: chr 12
allele count: 2
allele frequency: 1.699639676388606e-5
allele num: 117672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3380C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.56C>T
  hgvsp: ENSP00000460651.1:p.Pro19Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3380C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2159C>T
  hgvsp: ENSP00000444465.1:p.Pro720Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5615C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2414C>T
  hgvsp: ENSP00000433548.2:p.Pro805Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3380C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3380C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5615C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro720Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

12-977052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977052
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977052
    reference: chr 12
allele count: 7
allele frequency: 5.931499652583592e-5
allele num: 118014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.57G>A
  hgvsp: ENST00000574564.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2415G>A
  hgvsp: ENST00000530271.2:c.2415G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3379G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2160G>A
  hgvsp: ENST00000537687.1:c.2160G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5616G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3379G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3379G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5616G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3379G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38772
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Pro720Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

12-977057-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977057
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977057
    reference: chr 12
allele count: 1
allele frequency: 8.414108777598277e-6
allele num: 118848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3374G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2420G>C
  hgvsp: ENSP00000433548.2:p.Gly807Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3374G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5621G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3374G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.62G>C
  hgvsp: ENSP00000460651.1:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2165G>C
  hgvsp: ENSP00000444465.1:p.Gly722Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3374G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5621G>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly722Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

12-977070-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977070
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977070
    reference: chr 12
allele count: 2
allele frequency: 1.666638889351844e-5
allele num: 120002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.75A>T
  hgvsp: ENST00000574564.1:c.75A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2433A>T
  hgvsp: ENST00000530271.2:c.2433A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3361A>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3361A>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2178A>T
  hgvsp: ENST00000537687.1:c.2178A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3361A>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3361A>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5634A>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5634A>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51586
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr726Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-977096-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977096
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977096
    reference: chr 12
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.101C>A
  hgvsp: ENSP00000460651.1:p.Pro34Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3335C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2204C>A
  hgvsp: ENSP00000444465.1:p.Pro735Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5660C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2459C>A
  hgvsp: ENSP00000433548.2:p.Pro820Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3335C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5660C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3335C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3335C>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro735Gln
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: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

12-977097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977097
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977097
    reference: chr 12
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3334A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3334A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5661A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.102A>G
  hgvsp: ENST00000574564.1:c.102A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5661A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2205A>G
  hgvsp: ENST00000537687.1:c.2205A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2460A>G
  hgvsp: ENST00000530271.2:c.2460A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3334A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3334A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro735Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

12-977098-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977098
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977098
    reference: chr 12
allele count: 3
allele frequency: 2.486984779653149e-5
allele num: 120628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2206A>G
  hgvsp: ENSP00000444465.1:p.Thr736Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3333A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5662A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2461A>G
  hgvsp: ENSP00000433548.2:p.Thr821Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3333A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.103A>G
  hgvsp: ENSP00000460651.1:p.Thr35Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5662A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3333A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3333A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr736Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

12-977101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977101
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977101
    reference: chr 12
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2209A>G
  hgvsp: ENSP00000444465.1:p.Ile737Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2464A>G
  hgvsp: ENSP00000433548.2:p.Ile822Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3330A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3330A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5665A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3330A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5665A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.106A>G
  hgvsp: ENSP00000460651.1:p.Ile36Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3330A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3814
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile737Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

12-977102-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977102
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977102
    reference: chr 12
allele count: 3
allele frequency: 2.486861083939851e-5
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3329T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3329T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.107T>C
  hgvsp: ENSP00000460651.1:p.Ile36Thr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2465T>C
  hgvsp: ENSP00000433548.2:p.Ile822Thr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2210T>C
  hgvsp: ENSP00000444465.1:p.Ile737Thr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5666T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3329T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3329T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5666T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile737Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

12-977111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977111
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977111
    reference: chr 12
allele count: 3
allele frequency: 2.485830764641543e-5
allele num: 120684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2219G>A
  hgvsp: ENSP00000444465.1:p.Arg740His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3320G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3320G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5675G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5675G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3320G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2474G>A
  hgvsp: ENSP00000433548.2:p.Arg825His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.116G>A
  hgvsp: ENSP00000460651.1:p.Arg39His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3320G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52741
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg740His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-977115-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977115
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977115
    reference: chr 12
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3316A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3316A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2478A>C
  hgvsp: ENST00000530271.2:c.2478A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3316A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2223A>C
  hgvsp: ENST00000537687.1:c.2223A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3316A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.120A>C
  hgvsp: ENST00000574564.1:c.120A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5679A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5679A>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3808
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro741Pro
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

12-977119-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977119
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977119
    reference: chr 12
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5683T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3312T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2227T>G
  hgvsp: ENSP00000444465.1:p.Ser743Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2482T>G
  hgvsp: ENSP00000433548.2:p.Ser828Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3312T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3312T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.124T>G
  hgvsp: ENSP00000460651.1:p.Ser42Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3312T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5683T>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16793
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser743Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

12-977126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977126
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977126
    reference: chr 12
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5690C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3305C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2234C>T
  hgvsp: ENSP00000444465.1:p.Ser745Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3305C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5690C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.131C>T
  hgvsp: ENSP00000460651.1:p.Ser44Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2489C>T
  hgvsp: ENSP00000433548.2:p.Ser830Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3305C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3305C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser745Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-977127-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977127
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977127
    reference: chr 12
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5691A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2490A>G
  hgvsp: ENST00000530271.2:c.2490A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2235A>G
  hgvsp: ENST00000537687.1:c.2235A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3304A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.132A>G
  hgvsp: ENST00000574564.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3304A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5691A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3304A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3304A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser745Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

12-977133-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977133
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977133
    reference: chr 12
allele count: 2
allele frequency: 1.656397005234214e-5
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2496T>C
  hgvsp: ENST00000530271.2:c.2496T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2241T>C
  hgvsp: ENST00000537687.1:c.2241T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3298T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3298T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5697T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.138T>C
  hgvsp: ENST00000574564.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3298T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5697T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3298T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52838
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro747Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

12-977137-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977137
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977137
    reference: chr 12
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.142A>G
  hgvsp: ENSP00000460651.1:p.Thr48Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3294A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5701A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5701A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2500A>G
  hgvsp: ENSP00000433548.2:p.Thr834Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2245A>G
  hgvsp: ENSP00000444465.1:p.Thr749Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3294A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3294A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3294A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3797
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr749Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

12-977141-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977141
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977141
    reference: chr 12
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3290G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5705G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5705G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.146G>T
  hgvsp: ENSP00000460651.1:p.Cys49Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2249G>T
  hgvsp: ENSP00000444465.1:p.Cys750Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3290G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2504G>T
  hgvsp: ENSP00000433548.2:p.Cys835Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3290G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3290G>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys750Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-977141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977141
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977141
    reference: chr 12
allele count: 2
allele frequency: 1.656259834042764e-5
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5705G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3290G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2249G>A
  hgvsp: ENSP00000444465.1:p.Cys750Tyr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5705G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3290G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2504G>A
  hgvsp: ENSP00000433548.2:p.Cys835Tyr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.146G>A
  hgvsp: ENSP00000460651.1:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3290G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3290G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys750Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

12-977147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977147
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977147
    reference: chr 12
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3284C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5711C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2255C>T
  hgvsp: ENSP00000444465.1:p.Pro752Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3284C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3284C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.152C>T
  hgvsp: ENSP00000460651.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5711C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3284C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2510C>T
  hgvsp: ENSP00000433548.2:p.Pro837Leu
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro752Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-977152-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977152
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977152
    reference: chr 12
allele count: 4
allele frequency: 3.312355084465055e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3279G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5716G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3279G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2515G>T
  hgvsp: ENSP00000433548.2:p.Val839Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5716G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2260G>T
  hgvsp: ENSP00000444465.1:p.Val754Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3279G>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.157G>T
  hgvsp: ENSP00000460651.1:p.Val53Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3279G>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val754Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-977155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977155
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977155
    reference: chr 12
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2518G>A
  hgvsp: ENSP00000433548.2:p.Ala840Thr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3276G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3276G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3276G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5719G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2263G>A
  hgvsp: ENSP00000444465.1:p.Ala755Thr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5719G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.160G>A
  hgvsp: ENSP00000460651.1:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3276G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52890
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala755Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

12-977157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977157
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977157
    reference: chr 12
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3274C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2520C>T
  hgvsp: ENST00000530271.2:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3274C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5721C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2265C>T
  hgvsp: ENST00000537687.1:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3274C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5721C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3274C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.162C>T
  hgvsp: ENST00000574564.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala755Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

12-977158-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977158
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977158
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3273A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5722A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.163A>G
  hgvsp: ENSP00000460651.1:p.Ile55Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3273A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2266A>G
  hgvsp: ENSP00000444465.1:p.Ile756Val
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3273A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3273A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5722A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2521A>G
  hgvsp: ENSP00000433548.2:p.Ile841Val
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52890
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile756Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

12-977168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977168
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977168
    reference: chr 12
allele count: 3
allele frequency: 2.484430899695243e-5
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3263G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.173G>A
  hgvsp: ENSP00000460651.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3263G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5732G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5732G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2276G>A
  hgvsp: ENSP00000444465.1:p.Arg759Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2531G>A
  hgvsp: ENSP00000433548.2:p.Arg844Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3263G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3263G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg759Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

12-977170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977170
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977170
    reference: chr 12
allele count: 21
allele frequency: 1.73910162978667e-4
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2278C>T
  hgvsp: ENSP00000444465.1:p.Arg760Cys
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3261C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2533C>T
  hgvsp: ENSP00000433548.2:p.Arg845Cys
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5734C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3261C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.175C>T
  hgvsp: ENSP00000460651.1:p.Arg59Cys
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3261C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5734C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3261C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16879
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg760Cys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-977193-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977193
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977193
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3238A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2301A>G
  hgvsp: ENST00000537687.1:c.2301A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5757A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3238A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.198A>G
  hgvsp: ENST00000574564.1:c.198A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3238A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5757A>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2556A>G
  hgvsp: ENST00000530271.2:c.2556A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3238A>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3803
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu767Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

12-977205-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977205
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977205
    reference: chr 12
allele count: 8
allele frequency: 6.624600453785131e-5
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3226C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2568C>T
  hgvsp: ENST00000530271.2:c.2568C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5769C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2313C>T
  hgvsp: ENST00000537687.1:c.2313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3226C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.210C>T
  hgvsp: ENST00000574564.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3226C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5769C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3226C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His771His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/12-977205-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977205
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977205
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2568C>A
  hgvsp: ENSP00000433548.2:p.His856Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3226C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5769C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3226C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5769C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2313C>A
  hgvsp: ENSP00000444465.1:p.His771Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.210C>A
  hgvsp: ENSP00000460651.1:p.His70Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3226C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3226C>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His771Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

12-977205-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977205
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977205
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3226C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2568C>G
  hgvsp: ENSP00000433548.2:p.His856Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3226C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3226C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5769C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3226C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.210C>G
  hgvsp: ENSP00000460651.1:p.His70Gln
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5769C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2313C>G
  hgvsp: ENSP00000444465.1:p.His771Gln
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52850
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His771Gln
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

12-977211-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977211
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977211
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5775C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3220C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5775C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3220C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.216C>G
  hgvsp: ENSP00000460651.1:p.Phe72Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2319C>G
  hgvsp: ENSP00000444465.1:p.Phe773Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3220C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2574C>G
  hgvsp: ENSP00000433548.2:p.Phe858Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3220C>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe773Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

12-977211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977211
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977211
    reference: chr 12
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2574C>T
  hgvsp: ENST00000530271.2:c.2574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3220C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5775C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3220C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.216C>T
  hgvsp: ENST00000574564.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5775C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2319C>T
  hgvsp: ENST00000537687.1:c.2319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3220C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3220C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe773Phe
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-977217-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977217
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977217
    reference: chr 12
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3214C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5781C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.222C>G
  hgvsp: ENST00000574564.1:c.222C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2325C>G
  hgvsp: ENST00000537687.1:c.2325C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2580C>G
  hgvsp: ENST00000530271.2:c.2580C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3214C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3214C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5781C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3214C>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro775Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

12-977225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977225
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977225
    reference: chr 12
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5789G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3206G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2588G>A
  hgvsp: ENSP00000433548.2:p.Arg863Lys
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2333G>A
  hgvsp: ENSP00000444465.1:p.Arg778Lys
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3206G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3206G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.230G>A
  hgvsp: ENSP00000460651.1:p.Arg77Lys
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3206G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5789G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52868
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3795
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg778Lys
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

12-977228-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977228
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977228
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2591C>G
  hgvsp: ENSP00000433548.2:p.Thr864Ser
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5792C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3203C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5792C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2336C>G
  hgvsp: ENSP00000444465.1:p.Thr779Ser
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3203C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3203C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.233C>G
  hgvsp: ENSP00000460651.1:p.Thr78Ser
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3203C>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr779Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

12-977230-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977230
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977230
    reference: chr 12
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2593G>C
  hgvsp: ENSP00000433548.2:p.Val865Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5794G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3201G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5794G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3201G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3201G>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2338G>C
  hgvsp: ENSP00000444465.1:p.Val780Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.235G>C
  hgvsp: ENSP00000460651.1:p.Val79Leu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3201G>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val780Leu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

12-977231-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977231
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977231
    reference: chr 12
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5795T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3200T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2339T>C
  hgvsp: ENSP00000444465.1:p.Val780Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2594T>C
  hgvsp: ENSP00000433548.2:p.Val865Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5795T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3200T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3200T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.236T>C
  hgvsp: ENSP00000460651.1:p.Val79Ala
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3200T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val780Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

12-977235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977235
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977235
    reference: chr 12
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2598C>T
  hgvsp: ENST00000530271.2:c.2598C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2343C>T
  hgvsp: ENST00000537687.1:c.2343C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3196C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3196C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5799C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5799C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3196C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.240C>T
  hgvsp: ENST00000574564.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3196C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly781Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

12-977236-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977236
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977236
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2599C>G
  hgvsp: ENSP00000433548.2:p.Gln867Glu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5800C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3195C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3195C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5800C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2344C>G
  hgvsp: ENSP00000444465.1:p.Gln782Glu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.241C>G
  hgvsp: ENSP00000460651.1:p.Gln81Glu
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3195C>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3195C>G
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln782Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-977242-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977242
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977242
    reference: chr 12
allele count: 10
allele frequency: 8.280750567231414e-5
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.247C>A
  hgvsp: ENSP00000460651.1:p.Leu83Ile
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3189C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2605C>A
  hgvsp: ENSP00000433548.2:p.Leu869Ile
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3189C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2350C>A
  hgvsp: ENSP00000444465.1:p.Leu784Ile
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5806C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3189C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3189C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5806C>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52873
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu784Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

12-977242-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977242
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977242
    reference: chr 12
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3189C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2605C>T
  hgvsp: ENSP00000433548.2:p.Leu869Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3189C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3189C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5806C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2350C>T
  hgvsp: ENSP00000444465.1:p.Leu784Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.247C>T
  hgvsp: ENSP00000460651.1:p.Leu83Phe
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5806C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3189C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu784Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

12-977243-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977243
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977243
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3188T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2606T>C
  hgvsp: ENSP00000433548.2:p.Leu869Pro
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.248T>C
  hgvsp: ENSP00000460651.1:p.Leu83Pro
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3188T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3188T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5807T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5807T>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2351T>C
  hgvsp: ENSP00000444465.1:p.Leu784Pro
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3188T>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu784Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

12-977243-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977243
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977243
    reference: chr 12
allele count: 3
allele frequency: 2.484225170169424e-5
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2606T>G
  hgvsp: ENSP00000433548.2:p.Leu869Arg
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.248T>G
  hgvsp: ENSP00000460651.1:p.Leu83Arg
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3188T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5807T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3188T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5807T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3188T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3188T>G
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2351T>G
  hgvsp: ENSP00000444465.1:p.Leu784Arg
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52882
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu784Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-977245-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977245
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977245
    reference: chr 12
allele count: 3
allele frequency: 2.484225170169424e-5
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5809C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2353C>A
  hgvsp: ENSP00000444465.1:p.Leu785Ile
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3186C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3186C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2608C>A
  hgvsp: ENSP00000433548.2:p.Leu870Ile
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.250C>A
  hgvsp: ENSP00000460651.1:p.Leu84Ile
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3186C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5809C>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3186C>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu785Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-977269-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977269
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977269
    reference: chr 12
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3162A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5833A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2632A>C
  hgvsp: ENSP00000433548.2:p.Asn878His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3162A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5833A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.274A>C
  hgvsp: ENSP00000460651.1:p.Asn92His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2377A>C
  hgvsp: ENSP00000444465.1:p.Asn793His
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3162A>C
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3162A>C
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn793His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-977283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977283
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977283
    reference: chr 12
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2646G>A
  hgvsp: ENST00000530271.2:c.2646G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5847G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3148G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3148G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3148G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.288G>A
  hgvsp: ENST00000574564.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3148G>A
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2391G>A
  hgvsp: ENST00000537687.1:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5847G>A
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52910
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu797Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

12-977286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 977286
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 977286
    reference: chr 12
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000460651
  ensembl transcript: ENST00000574564
  gene symbol: WNK1
  hgvsc: ENST00000574564.1:c.291C>T
  hgvsp: ENST00000574564.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000438313
  ensembl transcript: ENST00000544965
  gene symbol: WNK1
  hgvsc: ENST00000544965.1:c.190+5850C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000444465
  ensembl transcript: ENST00000537687
  gene symbol: WNK1
  hgvsc: ENST00000537687.1:c.2394C>T
  hgvsp: ENST00000537687.1:c.2394C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000441972
  ensembl transcript: ENST00000535572
  gene symbol: WNK1
  hgvsc: ENST00000535572.1:c.2140-3145C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000439552
  ensembl transcript: ENST00000535698
  gene symbol: WNK1
  hgvsc: ENST00000535698.1:c.36+5850C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000433548
  ensembl transcript: ENST00000530271
  gene symbol: WNK1
  hgvsc: ENST00000530271.2:c.2649C>T
  hgvsp: ENST00000530271.2:c.2649C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000341292
  ensembl transcript: ENST00000340908
  gene symbol: WNK1
  hgvsc: ENST00000340908.4:c.919-3145C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000446462
  ensembl transcript: ENST00000545285
  gene symbol: WNK1
  hgvsc: ENST00000545285.1:c.98-3145C>T
  variant of: http://identifiers.org/hgnc/14540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000060237
  ensembl protein: ENSP00000313059
  ensembl transcript: ENST00000315939
  gene symbol: WNK1
  hgvsc: ENST00000315939.6:c.2140-3145C>T
  variant of: http://identifiers.org/hgnc/14540
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38336
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala798Ala
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4126
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3536
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.197e0

FS
type: SiteQuality
SIO_000300: 1.1867e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.77e-1

DP
type: SiteQuality
SIO_000300: 1.76203e5

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.47e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.05761316872428e-3
allele num: 486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.864e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.692e0

FS
type: SiteQuality
SIO_000300: 3.066e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.535e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.61e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

DP
type: SiteQuality
SIO_000300: 1.72315e5

VQSLOD
type: SiteQuality
SIO_000300: -2.759e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.895193977996526e-4
allele num: 3454
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 5.798e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.61e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

DP
type: SiteQuality
SIO_000300: 1.71899e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.299e0

QD
type: SiteQuality
SIO_000300: 7.22e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.242152466367713e-3
allele num: 446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

DP
type: SiteQuality
SIO_000300: 1.43027e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

QD
type: SiteQuality
SIO_000300: 8.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1812
bin: 6.25e1
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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variant carriers: 15

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
all individuals: 4
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variant carriers: 0

South Asian
type: Population
allele count: 16
allele frequency: 2.236511042773274e-3
allele num: 7154
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

QD
type: SiteQuality
SIO_000300: 1.484e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.32e-2

DP
type: SiteQuality
SIO_000300: 1.18175e5

GenotypeQuality
all individuals: 5692
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 191
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.808154630252909e-5
allele num: 41596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.450980392156863e-4
allele num: 4080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.33901e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

QD
type: SiteQuality
SIO_000300: 9.23e0

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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variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6882
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12618
num of homozygotes: 0

East Asian
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: 608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4098
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 41624
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4084
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6870
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.932730445819452e-5
allele num: 12606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 7.926442612555485e-5
allele num: 12616
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 41670
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 608
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East Asian
type: Population
allele count: 0
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allele num: 5502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.43353e5

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.11e0

MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 4
allele frequency: 7.160759040458289e-4
allele num: 5586
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.58782e5

FS
type: SiteQuality
SIO_000300: 3.774e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 1.477e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.686395080707149e-5
allele num: 13010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5874
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.14e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 4.464e0

DP
type: SiteQuality
SIO_000300: 9.51095e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.088474590130423e-5
allele num: 48918
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

FS
type: SiteQuality
SIO_000300: 3.857e0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.064265e6

QD
type: SiteQuality
SIO_000300: 1.63e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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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: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.044237295065211e-5
allele num: 48918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4880
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.63e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.857e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

DP
type: SiteQuality
SIO_000300: 1.064265e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 169
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variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.021999352960207e-5
allele num: 49456
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.533569799847986e-4
allele num: 7894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4934
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.682e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 1.093e0

DP
type: SiteQuality
SIO_000300: 1.076468e6

QD
type: SiteQuality
SIO_000300: 9.16e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1912
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.929310078715851e-5
allele num: 51832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13942
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.122908e6

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.583e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.167e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.455e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2406
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GenotypeQuality
all individuals: 363
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52914
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.463700234192037e-4
allele num: 6832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

DP
type: SiteQuality
SIO_000300: 1.144753e6

FS
type: SiteQuality
SIO_000300: 1.603e0

MQRankSum
type: SiteQuality
SIO_000300: -1.692e0

QD
type: SiteQuality
SIO_000300: 1.554e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 375
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.854009595613433e-5
allele num: 14590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.569134128060533e-5
allele num: 56036
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

QD
type: SiteQuality
SIO_000300: 1.396e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 1.208436e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2696
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GenotypeQuality
all individuals: 548
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.372495196266813e-4
allele num: 7286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57256
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5740
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.23626e6

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

FS
type: SiteQuality
SIO_000300: 3.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 9.6e0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
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GenotypeQuality
all individuals: 737
bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 1382
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 5658
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 394
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GenotypeQuality
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GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.109631602308034e-4
allele num: 9012
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15410
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.272e1

MQ
type: SiteQuality
SIO_000300: 5.477e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.325892e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.385e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.238e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.862e0

GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63456
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.315523556902867e-5
allele num: 15834
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

FS
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

DP
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QD
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MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.45e-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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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.298815822625347e-5
allele num: 15876
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

East Asian
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: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569267465946896e-5
allele num: 63724
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.572e1

DP
type: SiteQuality
SIO_000300: 1.386137e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 7.595e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.147e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566563273490616e-5
allele num: 63834
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.098e1

DP
type: SiteQuality
SIO_000300: 1.389355e6

VQSLOD
type: SiteQuality
SIO_000300: -2.247e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 2.78e0

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

MQ
type: SiteQuality
SIO_000300: 5.843e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.355e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.850823616509347e-4
allele num: 10806
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.324e0

FS
type: SiteQuality
SIO_000300: 6.616e0

QD
type: SiteQuality
SIO_000300: 1.29e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.394e0

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

DP
type: SiteQuality
SIO_000300: 1.401238e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.842638658559057e-4
allele num: 10854
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8292
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

European (Finnish)
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: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64298
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.034e1

FS
type: SiteQuality
SIO_000300: 5.931e0

DP
type: SiteQuality
SIO_000300: 1.412264e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.55e0

ReadPosRankSum
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SIO_000300: 6.42e-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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bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

Other
type: Population
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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: 3.070404372255826e-5
allele num: 65138
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11100
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.42784e6

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.1677e1

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.004e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-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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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
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European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.12369871402327e-5
allele num: 65320
num of homozygotes: 0

Other
type: Population
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Latino
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South Asian
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allele frequency: 1.848884506347837e-4
allele num: 16226
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East Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 6.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

DP
type: SiteQuality
SIO_000300: 1.433102e6

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.96e-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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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520820026158104e-5
allele num: 65754
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

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

Other
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.447726e6

FS
type: SiteQuality
SIO_000300: 7.067e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 8.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-1

QD
type: SiteQuality
SIO_000300: 2.41e0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.059732234809475e-4
allele num: 9710
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

FS
type: SiteQuality
SIO_000300: 2.246e0

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.426e1

DP
type: SiteQuality
SIO_000300: 1.464722e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 820
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-2

QD
type: SiteQuality
SIO_000300: 1.206e1

DP
type: SiteQuality
SIO_000300: 1.479647e6

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 9.25e1
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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variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: -2.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.479663e6

QD
type: SiteQuality
SIO_000300: 1.178e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1161
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 218
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000390050706592e-5
allele num: 66658
num of homozygotes: 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: 11560
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.115e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

FS
type: SiteQuality
SIO_000300: 2.528e0

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

MQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

DP
type: SiteQuality
SIO_000300: 1.479932e6

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 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: 8616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.838e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

DP
type: SiteQuality
SIO_000300: 1.480735e6

FS
type: SiteQuality
SIO_000300: 7.973e0

QD
type: SiteQuality
SIO_000300: 1.66e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

GenotypeQuality
all individuals: 3816
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
all individuals: 810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817741153659719e-4
allele num: 16504
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
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: 896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

QD
type: SiteQuality
SIO_000300: 1.121e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

DP
type: SiteQuality
SIO_000300: 1.48088e6

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

FS
type: SiteQuality
SIO_000300: 5.835e0

VQSLOD
type: SiteQuality
SIO_000300: 7.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 800
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GenotypeQuality
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GenotypeQuality
all individuals: 215
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
all individuals: 15
bin: 3.75e1
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 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: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998500749625187e-5
allele num: 66700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
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: 11556
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 3.119e0

QD
type: SiteQuality
SIO_000300: 1.165e1

DP
type: SiteQuality
SIO_000300: 1.481453e6

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

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

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 8
bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 18
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 855
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GenotypeQuality
all individuals: 52778
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.481426e6

FS
type: SiteQuality
SIO_000300: 7.989e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.151e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.26e1

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
all individuals: 11
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GenotypeQuality
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GenotypeQuality
all individuals: 187
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 857
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GenotypeQuality
all individuals: 804
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variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

FS
type: SiteQuality
SIO_000300: 3.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.41e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

DP
type: SiteQuality
SIO_000300: 1.481464e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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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bin: 1.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 3.434e0

MQRankSum
type: SiteQuality
SIO_000300: -1.357e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.481663e6

QD
type: SiteQuality
SIO_000300: 1.583e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.285e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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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GenotypeQuality
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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: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.601e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: -1.643e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.481658e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 5.42e0

QD
type: SiteQuality
SIO_000300: 8.92e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.523e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

African
type: Population
allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.157e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e0

FS
type: SiteQuality
SIO_000300: 9.231999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 1.481558e6

QD
type: SiteQuality
SIO_000300: 1.37e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.871e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

GenotypeQuality
all individuals: 865
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.648e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

QD
type: SiteQuality
SIO_000300: 1.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
SIO_000300: 1.481594e6

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

FS
type: SiteQuality
SIO_000300: 4.564e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3
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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: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
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: 898
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.374e0

DP
type: SiteQuality
SIO_000300: 1.481794e6

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.072e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.353e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
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: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.072e0

FS
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

DP
type: SiteQuality
SIO_000300: 1.481794e6

QD
type: SiteQuality
SIO_000300: 1.353e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9798
num of homozygotes: 0

Other
type: Population
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South Asian
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East Asian
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allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

FS
type: SiteQuality
SIO_000300: 1.764e0

QD
type: SiteQuality
SIO_000300: 1.849e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-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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bin: 4.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.017e0

FS
type: SiteQuality
SIO_000300: 3.755e0

DP
type: SiteQuality
SIO_000300: 1.482384e6

QD
type: SiteQuality
SIO_000300: 1.364e1

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

QD
type: SiteQuality
SIO_000300: 1.731e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.933e0

FS
type: SiteQuality
SIO_000300: 1.409e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e0

DP
type: SiteQuality
SIO_000300: 1.481809e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 1.261e0

QD
type: SiteQuality
SIO_000300: 7.19e0

VQSLOD
type: SiteQuality
SIO_000300: -9.468e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

DP
type: SiteQuality
SIO_000300: 1.481731e6

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 898
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 1.48167e6

FS
type: SiteQuality
SIO_000300: 2.871e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.497e0

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 431
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variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.481953e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.357e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 868
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 9.75e1
variant carriers: 21

Latino
type: Population
allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.547274416374479e-4
allele num: 66738
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.91e0

DP
type: SiteQuality
SIO_000300: 1.483822e6

FS
type: SiteQuality
SIO_000300: 5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

QD
type: SiteQuality
SIO_000300: 1.274e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.14e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.48173e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

FS
type: SiteQuality
SIO_000300: 1.371e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

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

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

QD
type: SiteQuality
SIO_000300: 1.435e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8

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: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.91085003455425e-4
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

FS
type: SiteQuality
SIO_000300: 1.855e0

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

DP
type: SiteQuality
SIO_000300: 1.482791e6

QD
type: SiteQuality
SIO_000300: 1.005e1

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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variant carriers: 0

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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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.482791e6

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.81e-1

QD
type: SiteQuality
SIO_000300: 1.005e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.695e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

FS
type: SiteQuality
SIO_000300: 1.855e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 190
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GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3798
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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SIO_000300: -3.695e0

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -8.81e-1

QD
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

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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African
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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

East Asian
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allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

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

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

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

East Asian
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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QD
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FS
type: SiteQuality
SIO_000300: 5.3e-1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.01e0

ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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SIO_000300: -1.1e-2

BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 6.51e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 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

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

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

ClippingRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -4.796e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

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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East Asian
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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
allele num: 9798
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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Latino
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East Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

MQ
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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DP
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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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East Asian
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

VQSLOD
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SIO_000300: 3.11e-1

DP
type: SiteQuality
SIO_000300: 1.481699e6

MQRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 9.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.076e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.48167e6

VQSLOD
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SIO_000300: -1.604e-1

BaseQRankSum
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SIO_000300: -2.596e0

MQRankSum
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SIO_000300: 9.85e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

FS
type: SiteQuality
SIO_000300: 6.836e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

Other
type: Population
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allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.198681450404555e-4
allele num: 66740
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

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

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

ClippingRankSum
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SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.127e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -4.04e0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

DP
type: SiteQuality
SIO_000300: 1.483371e6

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-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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variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.127e1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

BaseQRankSum
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SIO_000300: -4.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.483371e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

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: 1

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

DP
type: SiteQuality
SIO_000300: 1.482044e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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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Latino
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allele frequency: 0.0e0
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African
type: Population
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allele frequency: 3.062474479379339e-4
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Other
type: Population
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FS
type: SiteQuality
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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South Asian
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East Asian
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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MQ
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VQSLOD
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DP
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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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variant carriers: 0

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

South Asian
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East Asian
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Latino
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European (Non-Finnish)
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Other
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African
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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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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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
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African
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European (Finnish)
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Latino
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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 frequency: 1.498351813005694e-5
allele num: 66740
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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DP
type: SiteQuality
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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