6-73904826-TTGTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904826
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904822
    reference: chr 6
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2522_2525delCTGT
  hgvsp: ENSP00000385501.2:p.Ser841CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2492_2495delCTGT
  hgvsp: ENSP00000347326.4:p.Ser831CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2162_2165delCTGT
  hgvsp: ENSP00000409861.2:p.Ser721CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2549_2552delCTGT
  hgvsp: ENSP00000345055.2:p.Ser850CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2495_2498delCTGT
  hgvsp: ENSP00000347853.3:p.Ser832CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2492_2495delCTGT
  hgvsp: ENSP00000359425.1:p.Ser831CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2465_2468delCTGT
  hgvsp: ENSP00000384453.2:p.Ser822CysfsTer4
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8175
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23789
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser850CysfsTer4
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: TTGTC
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

6-73904834-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904834
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904834
    reference: chr 6
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2496G>C
  hgvsp: ENST00000355194.4:c.2496G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2469G>C
  hgvsp: ENST00000403813.2:c.2469G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2496G>C
  hgvsp: ENST00000370398.1:c.2496G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2499G>C
  hgvsp: ENST00000355635.3:c.2499G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2526G>C
  hgvsp: ENST00000402622.2:c.2526G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2553G>C
  hgvsp: ENST00000342056.2:c.2553G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2166G>C
  hgvsp: ENST00000414165.2:c.2166G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23759
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10003
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val851Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

6-73904843-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904843
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904843
    reference: chr 6
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2505G>T
  hgvsp: ENST00000355194.4:c.2505G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2562G>T
  hgvsp: ENST00000342056.2:c.2562G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2505G>T
  hgvsp: ENST00000370398.1:c.2505G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2175G>T
  hgvsp: ENST00000414165.2:c.2175G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2535G>T
  hgvsp: ENST00000402622.2:c.2535G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2508G>T
  hgvsp: ENST00000355635.3:c.2508G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2478G>T
  hgvsp: ENST00000403813.2:c.2478G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5382
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu854Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

6-73904849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904849
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904849
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2484G>A
  hgvsp: ENST00000403813.2:c.2484G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2181G>A
  hgvsp: ENST00000414165.2:c.2181G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2541G>A
  hgvsp: ENST00000402622.2:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2511G>A
  hgvsp: ENST00000370398.1:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2511G>A
  hgvsp: ENST00000355194.4:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2568G>A
  hgvsp: ENST00000342056.2:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2514G>A
  hgvsp: ENST00000355635.3:c.2514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10003
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg856Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

6-73904851-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904851
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904851
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2513C>T
  hgvsp: ENSP00000359425.1:p.Ser838Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2543C>T
  hgvsp: ENSP00000385501.2:p.Ser848Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2183C>T
  hgvsp: ENSP00000409861.2:p.Ser728Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2513C>T
  hgvsp: ENSP00000347326.4:p.Ser838Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2570C>T
  hgvsp: ENSP00000345055.2:p.Ser857Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2486C>T
  hgvsp: ENSP00000384453.2:p.Ser829Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2516C>T
  hgvsp: ENSP00000347853.3:p.Ser839Leu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10002
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser857Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

6-73904852-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904852
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904852
    reference: chr 6
allele count: 3
allele frequency: 2.472187886279357e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2571G>A
  hgvsp: ENST00000342056.2:c.2571G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2514G>A
  hgvsp: ENST00000370398.1:c.2514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2517G>A
  hgvsp: ENST00000355635.3:c.2517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2544G>A
  hgvsp: ENST00000402622.2:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2514G>A
  hgvsp: ENST00000355194.4:c.2514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2487G>A
  hgvsp: ENST00000403813.2:c.2487G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2184G>A
  hgvsp: ENST00000414165.2:c.2184G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser857Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-73904854-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904854
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904854
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2546C>T
  hgvsp: ENSP00000385501.2:p.Thr849Ile
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2573C>T
  hgvsp: ENSP00000345055.2:p.Thr858Ile
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2519C>T
  hgvsp: ENSP00000347853.3:p.Thr840Ile
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2489C>T
  hgvsp: ENSP00000384453.2:p.Thr830Ile
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2516C>T
  hgvsp: ENSP00000359425.1:p.Thr839Ile
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2516C>T
  hgvsp: ENSP00000347326.4:p.Thr839Ile
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2186C>T
  hgvsp: ENSP00000409861.2:p.Thr729Ile
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10779
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr858Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

6-73904855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904855
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904855
    reference: chr 6
allele count: 50
allele frequency: 4.120652711389484e-4
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2517C>T
  hgvsp: ENST00000370398.1:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2520C>T
  hgvsp: ENST00000355635.3:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2547C>T
  hgvsp: ENST00000402622.2:c.2547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2574C>T
  hgvsp: ENST00000342056.2:c.2574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2490C>T
  hgvsp: ENST00000403813.2:c.2490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2517C>T
  hgvsp: ENST00000355194.4:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2187C>T
  hgvsp: ENST00000414165.2:c.2187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16580
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10040
  bin: 9.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 5380
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr858Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

6-73904868-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904868
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904868
    reference: chr 6
allele count: 5
allele frequency: 4.120516877637131e-5
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2560A>G
  hgvsp: ENSP00000385501.2:p.Ile854Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2587A>G
  hgvsp: ENSP00000345055.2:p.Ile863Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2530A>G
  hgvsp: ENSP00000347326.4:p.Ile844Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2530A>G
  hgvsp: ENSP00000359425.1:p.Ile844Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2200A>G
  hgvsp: ENSP00000409861.2:p.Ile734Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2503A>G
  hgvsp: ENSP00000384453.2:p.Ile835Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2533A>G
  hgvsp: ENSP00000347853.3:p.Ile845Val
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23463
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile863Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

6-73904871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904871
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904871
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2536C>T
  hgvsp: ENSP00000347853.3:p.Gln846Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2203C>T
  hgvsp: ENSP00000409861.2:p.Gln735Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2533C>T
  hgvsp: ENSP00000347326.4:p.Gln845Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2533C>T
  hgvsp: ENSP00000359425.1:p.Gln845Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2590C>T
  hgvsp: ENSP00000345055.2:p.Gln864Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2506C>T
  hgvsp: ENSP00000384453.2:p.Gln836Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2563C>T
  hgvsp: ENSP00000385501.2:p.Gln855Ter
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8107
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5398
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4197
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23408
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln864Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

6-73904881-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904881
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904881
    reference: chr 6
allele count: 5
allele frequency: 4.120720631624058e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2543G>A
  hgvsp: ENSP00000347326.4:p.Gly848Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2546G>A
  hgvsp: ENSP00000347853.3:p.Gly849Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2543G>A
  hgvsp: ENSP00000359425.1:p.Gly848Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2213G>A
  hgvsp: ENSP00000409861.2:p.Gly738Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2573G>A
  hgvsp: ENSP00000385501.2:p.Gly858Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2516G>A
  hgvsp: ENSP00000384453.2:p.Gly839Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2600G>A
  hgvsp: ENSP00000345055.2:p.Gly867Glu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10030
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4217
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly867Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

6-73904882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904882
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904882
    reference: chr 6
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2544G>A
  hgvsp: ENST00000370398.1:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2544G>A
  hgvsp: ENST00000355194.4:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2214G>A
  hgvsp: ENST00000414165.2:c.2214G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2517G>A
  hgvsp: ENST00000403813.2:c.2517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2601G>A
  hgvsp: ENST00000342056.2:c.2601G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2547G>A
  hgvsp: ENST00000355635.3:c.2547G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2574G>A
  hgvsp: ENST00000402622.2:c.2574G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly867Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

6-73904890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904890
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904890
    reference: chr 6
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2582C>T
  hgvsp: ENSP00000385501.2:p.Ser861Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2552C>T
  hgvsp: ENSP00000347326.4:p.Ser851Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2609C>T
  hgvsp: ENSP00000345055.2:p.Ser870Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2555C>T
  hgvsp: ENSP00000347853.3:p.Ser852Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2222C>T
  hgvsp: ENSP00000409861.2:p.Ser741Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2525C>T
  hgvsp: ENSP00000384453.2:p.Ser842Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2552C>T
  hgvsp: ENSP00000359425.1:p.Ser851Leu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5425
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser870Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/6-73904891-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904891
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904891
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2553A>C
  hgvsp: ENST00000355194.4:c.2553A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2553A>C
  hgvsp: ENST00000370398.1:c.2553A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2526A>C
  hgvsp: ENST00000403813.2:c.2526A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2610A>C
  hgvsp: ENST00000342056.2:c.2610A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2583A>C
  hgvsp: ENST00000402622.2:c.2583A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2223A>C
  hgvsp: ENST00000414165.2:c.2223A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2556A>C
  hgvsp: ENST00000355635.3:c.2556A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23144
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser870Ser
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-73904895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904895
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904895
    reference: chr 6
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2557G>A
  hgvsp: ENSP00000347326.4:p.Gly853Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2557G>A
  hgvsp: ENSP00000359425.1:p.Gly853Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2530G>A
  hgvsp: ENSP00000384453.2:p.Gly844Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2587G>A
  hgvsp: ENSP00000385501.2:p.Gly863Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2227G>A
  hgvsp: ENSP00000409861.2:p.Gly743Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2560G>A
  hgvsp: ENSP00000347853.3:p.Gly854Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2614G>A
  hgvsp: ENSP00000345055.2:p.Gly872Ser
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22985
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly872Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-73904896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904896
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904896
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2228G>A
  hgvsp: ENSP00000409861.2:p.Gly743Asp
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2615G>A
  hgvsp: ENSP00000345055.2:p.Gly872Asp
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2561G>A
  hgvsp: ENSP00000347853.3:p.Gly854Asp
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2558G>A
  hgvsp: ENSP00000359425.1:p.Gly853Asp
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2558G>A
  hgvsp: ENSP00000347326.4:p.Gly853Asp
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2588G>A
  hgvsp: ENSP00000385501.2:p.Gly863Asp
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2531G>A
  hgvsp: ENSP00000384453.2:p.Gly844Asp
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5432
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly872Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

6-73904899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904899
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904899
    reference: chr 6
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2591C>T
  hgvsp: ENSP00000385501.2:p.Ser864Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2561C>T
  hgvsp: ENSP00000359425.1:p.Ser854Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2564C>T
  hgvsp: ENSP00000347853.3:p.Ser855Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2561C>T
  hgvsp: ENSP00000347326.4:p.Ser854Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2534C>T
  hgvsp: ENSP00000384453.2:p.Ser845Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2231C>T
  hgvsp: ENSP00000409861.2:p.Ser744Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2618C>T
  hgvsp: ENSP00000345055.2:p.Ser873Phe
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18447
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10055
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22796
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8087
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser873Phe
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-73904912-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904912
    reference: chr 6
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2604A>G
  hgvsp: ENST00000402622.2:c.2604A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2574A>G
  hgvsp: ENST00000355194.4:c.2574A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2574A>G
  hgvsp: ENST00000370398.1:c.2574A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2577A>G
  hgvsp: ENST00000355635.3:c.2577A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2631A>G
  hgvsp: ENST00000342056.2:c.2631A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2547A>G
  hgvsp: ENST00000403813.2:c.2547A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2244A>G
  hgvsp: ENST00000414165.2:c.2244A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10088
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4272
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln877Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

6-73904913-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904913
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904913
    reference: chr 6
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2548G>T
  hgvsp: ENSP00000384453.2:p.Asp850Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2575G>T
  hgvsp: ENSP00000359425.1:p.Asp859Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2575G>T
  hgvsp: ENSP00000347326.4:p.Asp859Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2632G>T
  hgvsp: ENSP00000345055.2:p.Asp878Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2245G>T
  hgvsp: ENSP00000409861.2:p.Asp749Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2605G>T
  hgvsp: ENSP00000385501.2:p.Asp869Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2578G>T
  hgvsp: ENSP00000347853.3:p.Asp860Tyr
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4218
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp878Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

6-73904915-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904915
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904915
    reference: chr 6
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2577T>C
  hgvsp: ENST00000370398.1:c.2577T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2247T>C
  hgvsp: ENST00000414165.2:c.2247T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2607T>C
  hgvsp: ENST00000402622.2:c.2607T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2580T>C
  hgvsp: ENST00000355635.3:c.2580T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2550T>C
  hgvsp: ENST00000403813.2:c.2550T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2577T>C
  hgvsp: ENST00000355194.4:c.2577T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2634T>C
  hgvsp: ENST00000342056.2:c.2634T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10092
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp878Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

6-73904920-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904920
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904920
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2582A>G
  hgvsp: ENSP00000359425.1:p.Tyr861Cys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2252A>G
  hgvsp: ENSP00000409861.2:p.Tyr751Cys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2639A>G
  hgvsp: ENSP00000345055.2:p.Tyr880Cys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2582A>G
  hgvsp: ENSP00000347326.4:p.Tyr861Cys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2585A>G
  hgvsp: ENSP00000347853.3:p.Tyr862Cys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2555A>G
  hgvsp: ENSP00000384453.2:p.Tyr852Cys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2612A>G
  hgvsp: ENSP00000385501.2:p.Tyr871Cys
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23027
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4222
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr880Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-73904924-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904924
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904924
    reference: chr 6
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2616C>A
  hgvsp: ENST00000402622.2:c.2616C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2589C>A
  hgvsp: ENST00000355635.3:c.2589C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2559C>A
  hgvsp: ENST00000403813.2:c.2559C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2643C>A
  hgvsp: ENST00000342056.2:c.2643C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2256C>A
  hgvsp: ENST00000414165.2:c.2256C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2586C>A
  hgvsp: ENST00000370398.1:c.2586C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2586C>A
  hgvsp: ENST00000355194.4:c.2586C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8160
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23015
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro881Pro
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: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

6-73904940-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904940
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904940
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2602A>G
  hgvsp: ENSP00000359425.1:p.Lys868Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2632A>G
  hgvsp: ENSP00000385501.2:p.Lys878Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2272A>G
  hgvsp: ENSP00000409861.2:p.Lys758Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2575A>G
  hgvsp: ENSP00000384453.2:p.Lys859Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2659A>G
  hgvsp: ENSP00000345055.2:p.Lys887Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2605A>G
  hgvsp: ENSP00000347853.3:p.Lys869Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2602A>G
  hgvsp: ENSP00000347326.4:p.Lys868Glu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10995
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23082
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys887Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

6-73904946-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904946
    reference: chr 6
allele count: 5
allele frequency: 4.119837843182493e-5
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2608T>C
  hgvsp: ENSP00000359425.1:p.Phe870Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2665T>C
  hgvsp: ENSP00000345055.2:p.Phe889Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2638T>C
  hgvsp: ENSP00000385501.2:p.Phe880Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2608T>C
  hgvsp: ENSP00000347326.4:p.Phe870Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2278T>C
  hgvsp: ENSP00000409861.2:p.Phe760Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2581T>C
  hgvsp: ENSP00000384453.2:p.Phe861Leu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2611T>C
  hgvsp: ENSP00000347853.3:p.Phe871Leu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10129
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4246
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe889Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

6-73904948-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904948
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904948
    reference: chr 6
allele count: 7
allele frequency: 5.767392808885081e-5
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2640T>C
  hgvsp: ENST00000402622.2:c.2640T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2583T>C
  hgvsp: ENST00000403813.2:c.2583T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2610T>C
  hgvsp: ENST00000355194.4:c.2610T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2610T>C
  hgvsp: ENST00000370398.1:c.2610T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2280T>C
  hgvsp: ENST00000414165.2:c.2280T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2667T>C
  hgvsp: ENST00000342056.2:c.2667T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2613T>C
  hgvsp: ENST00000355635.3:c.2613T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16583
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe889Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/6-73904953-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904953
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904953
    reference: chr 6
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2672C>A
  hgvsp: ENSP00000345055.2:p.Thr891Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2645C>A
  hgvsp: ENSP00000385501.2:p.Thr882Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2618C>A
  hgvsp: ENSP00000347853.3:p.Thr873Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2285C>A
  hgvsp: ENSP00000409861.2:p.Thr762Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2615C>A
  hgvsp: ENSP00000347326.4:p.Thr872Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2588C>A
  hgvsp: ENSP00000384453.2:p.Thr863Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2615C>A
  hgvsp: ENSP00000359425.1:p.Thr872Asn
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5523
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr891Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

6-73904953-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904953
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904953
    reference: chr 6
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2672C>G
  hgvsp: ENSP00000345055.2:p.Thr891Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2588C>G
  hgvsp: ENSP00000384453.2:p.Thr863Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2285C>G
  hgvsp: ENSP00000409861.2:p.Thr762Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2645C>G
  hgvsp: ENSP00000385501.2:p.Thr882Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2615C>G
  hgvsp: ENSP00000359425.1:p.Thr872Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2618C>G
  hgvsp: ENSP00000347853.3:p.Thr873Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2615C>G
  hgvsp: ENSP00000347326.4:p.Thr872Ser
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr891Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

6-73904954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904954
    reference: chr 6
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2616T>C
  hgvsp: ENST00000370398.1:c.2616T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2646T>C
  hgvsp: ENST00000402622.2:c.2646T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2619T>C
  hgvsp: ENST00000355635.3:c.2619T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2616T>C
  hgvsp: ENST00000355194.4:c.2616T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2286T>C
  hgvsp: ENST00000414165.2:c.2286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2589T>C
  hgvsp: ENST00000403813.2:c.2589T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2673T>C
  hgvsp: ENST00000342056.2:c.2673T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5523
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr891Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

6-73904957-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904957
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904957
    reference: chr 6
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2622T>C
  hgvsp: ENST00000355635.3:c.2622T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2619T>C
  hgvsp: ENST00000355194.4:c.2619T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2592T>C
  hgvsp: ENST00000403813.2:c.2592T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2649T>C
  hgvsp: ENST00000402622.2:c.2649T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2619T>C
  hgvsp: ENST00000370398.1:c.2619T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2676T>C
  hgvsp: ENST00000342056.2:c.2676T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2289T>C
  hgvsp: ENST00000414165.2:c.2289T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23089
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10132
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp892Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-73904960-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904960
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904960
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2622A>G
  hgvsp: ENST00000355194.4:c.2622A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2595A>G
  hgvsp: ENST00000403813.2:c.2595A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2652A>G
  hgvsp: ENST00000402622.2:c.2652A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2292A>G
  hgvsp: ENST00000414165.2:c.2292A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2622A>G
  hgvsp: ENST00000370398.1:c.2622A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2625A>G
  hgvsp: ENST00000355635.3:c.2625A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2679A>G
  hgvsp: ENST00000342056.2:c.2679A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu893Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

6-73904963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904963
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904963
    reference: chr 6
allele count: 6
allele frequency: 4.943398091848337e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2295G>A
  hgvsp: ENST00000414165.2:c.2295G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2625G>A
  hgvsp: ENST00000355194.4:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2598G>A
  hgvsp: ENST00000403813.2:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2682G>A
  hgvsp: ENST00000342056.2:c.2682G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2655G>A
  hgvsp: ENST00000402622.2:c.2655G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2625G>A
  hgvsp: ENST00000370398.1:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2628G>A
  hgvsp: ENST00000355635.3:c.2628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10138
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23094
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu894Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

6-73904964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904964
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904964
    reference: chr 6
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2296G>A
  hgvsp: ENSP00000409861.2:p.Val766Met
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2599G>A
  hgvsp: ENSP00000384453.2:p.Val867Met
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2656G>A
  hgvsp: ENSP00000385501.2:p.Val886Met
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2626G>A
  hgvsp: ENSP00000359425.1:p.Val876Met
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2626G>A
  hgvsp: ENSP00000347326.4:p.Val876Met
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2683G>A
  hgvsp: ENSP00000345055.2:p.Val895Met
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2629G>A
  hgvsp: ENSP00000347853.3:p.Val877Met
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5521
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val895Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD

6-73904972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904972
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904972
    reference: chr 6
allele count: 13
allele frequency: 1.071140187531928e-4
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2304C>T
  hgvsp: ENST00000414165.2:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2634C>T
  hgvsp: ENST00000355194.4:c.2634C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2637C>T
  hgvsp: ENST00000355635.3:c.2637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2607C>T
  hgvsp: ENST00000403813.2:c.2607C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2664C>T
  hgvsp: ENST00000402622.2:c.2664C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2691C>T
  hgvsp: ENST00000342056.2:c.2691C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2634C>T
  hgvsp: ENST00000370398.1:c.2634C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10149
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro897Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-73904973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904973
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904973
    reference: chr 6
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2635G>A
  hgvsp: ENSP00000347326.4:p.Glu879Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2608G>A
  hgvsp: ENSP00000384453.2:p.Glu870Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2665G>A
  hgvsp: ENSP00000385501.2:p.Glu889Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2692G>A
  hgvsp: ENSP00000345055.2:p.Glu898Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2638G>A
  hgvsp: ENSP00000347853.3:p.Glu880Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2635G>A
  hgvsp: ENSP00000359425.1:p.Glu879Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2305G>A
  hgvsp: ENSP00000409861.2:p.Glu769Lys
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu898Lys
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

6-73904976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904976
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904976
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2695G>A
  hgvsp: ENSP00000345055.2:p.Glu899Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2668G>A
  hgvsp: ENSP00000385501.2:p.Glu890Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2308G>A
  hgvsp: ENSP00000409861.2:p.Glu770Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2641G>A
  hgvsp: ENSP00000347853.3:p.Glu881Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2638G>A
  hgvsp: ENSP00000359425.1:p.Glu880Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2638G>A
  hgvsp: ENSP00000347326.4:p.Glu880Lys
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2611G>A
  hgvsp: ENSP00000384453.2:p.Glu871Lys
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu899Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-73904980-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904980
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904981
    reference: chr 6
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2643dupA
  hgvsp: ENSP00000359425.1:p.Glu882ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2616dupA
  hgvsp: ENSP00000384453.2:p.Glu873ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2700dupA
  hgvsp: ENSP00000345055.2:p.Glu901ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2643dupA
  hgvsp: ENSP00000347326.4:p.Glu882ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2646dupA
  hgvsp: ENSP00000347853.3:p.Glu883ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2313dupA
  hgvsp: ENSP00000409861.2:p.Glu772ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2673dupA
  hgvsp: ENSP00000385501.2:p.Glu892ArgfsTer6
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10150
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23094
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu901ArgfsTer6
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/6-73904990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904990
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904990
    reference: chr 6
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2322C>A
  hgvsp: ENSP00000409861.2:p.Asp774Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2655C>A
  hgvsp: ENSP00000347853.3:p.Asp885Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2652C>A
  hgvsp: ENSP00000347326.4:p.Asp884Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2682C>A
  hgvsp: ENSP00000385501.2:p.Asp894Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2709C>A
  hgvsp: ENSP00000345055.2:p.Asp903Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2625C>A
  hgvsp: ENSP00000384453.2:p.Asp875Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2652C>A
  hgvsp: ENSP00000359425.1:p.Asp884Glu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4238
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2792
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5516
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp903Glu
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-73904992-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73904992
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73904992
    reference: chr 6
allele count: 5
allele frequency: 4.119566292060772e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2711C>A
  hgvsp: ENSP00000345055.2:p.Thr904Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2654C>A
  hgvsp: ENSP00000359425.1:p.Thr885Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2654C>A
  hgvsp: ENSP00000347326.4:p.Thr885Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2684C>A
  hgvsp: ENSP00000385501.2:p.Thr895Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2657C>A
  hgvsp: ENSP00000347853.3:p.Thr886Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2324C>A
  hgvsp: ENSP00000409861.2:p.Thr775Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2627C>A
  hgvsp: ENSP00000384453.2:p.Thr876Asn
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2792
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8173
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr904Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

6-73905003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905003
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905003
    reference: chr 6
allele count: 5
allele frequency: 4.120720631624058e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2665G>A
  hgvsp: ENSP00000347326.4:p.Ala889Thr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2668G>A
  hgvsp: ENSP00000347853.3:p.Ala890Thr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2695G>A
  hgvsp: ENSP00000385501.2:p.Ala899Thr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2665G>A
  hgvsp: ENSP00000359425.1:p.Ala889Thr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2335G>A
  hgvsp: ENSP00000409861.2:p.Ala779Thr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2638G>A
  hgvsp: ENSP00000384453.2:p.Ala880Thr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2722G>A
  hgvsp: ENSP00000345055.2:p.Ala908Thr
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4235
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala908Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

6-73905003-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905003
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905003
    reference: chr 6
allele count: 5
allele frequency: 4.120720631624058e-5
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2722G>T
  hgvsp: ENSP00000345055.2:p.Ala908Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2638G>T
  hgvsp: ENSP00000384453.2:p.Ala880Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2668G>T
  hgvsp: ENSP00000347853.3:p.Ala890Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2335G>T
  hgvsp: ENSP00000409861.2:p.Ala779Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2665G>T
  hgvsp: ENSP00000347326.4:p.Ala889Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2665G>T
  hgvsp: ENSP00000359425.1:p.Ala889Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2695G>T
  hgvsp: ENSP00000385501.2:p.Ala899Ser
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4235
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala908Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

6-73905005-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905005
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905005
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2667A>G
  hgvsp: ENST00000370398.1:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2724A>G
  hgvsp: ENST00000342056.2:c.2724A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2667A>G
  hgvsp: ENST00000355194.4:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2670A>G
  hgvsp: ENST00000355635.3:c.2670A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2697A>G
  hgvsp: ENST00000402622.2:c.2697A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2337A>G
  hgvsp: ENST00000414165.2:c.2337A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2640A>G
  hgvsp: ENST00000403813.2:c.2640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala908Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-73905007-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905007
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905007
    reference: chr 6
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2699C>G
  hgvsp: ENSP00000385501.2:p.Pro900Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2672C>G
  hgvsp: ENSP00000347853.3:p.Pro891Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2669C>G
  hgvsp: ENSP00000347326.4:p.Pro890Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2642C>G
  hgvsp: ENSP00000384453.2:p.Pro881Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2669C>G
  hgvsp: ENSP00000359425.1:p.Pro890Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2726C>G
  hgvsp: ENSP00000345055.2:p.Pro909Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2339C>G
  hgvsp: ENSP00000409861.2:p.Pro780Arg
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23001
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10155
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro909Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

6-73905008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905008
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905008
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2643G>A
  hgvsp: ENST00000403813.2:c.2643G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2700G>A
  hgvsp: ENST00000402622.2:c.2700G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2670G>A
  hgvsp: ENST00000370398.1:c.2670G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2340G>A
  hgvsp: ENST00000414165.2:c.2340G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2727G>A
  hgvsp: ENST00000342056.2:c.2727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2670G>A
  hgvsp: ENST00000355194.4:c.2670G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2673G>A
  hgvsp: ENST00000355635.3:c.2673G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5505
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8146
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro909Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-73905017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905017
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905017
    reference: chr 6
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2679C>T
  hgvsp: ENST00000355194.4:c.2679C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2349C>T
  hgvsp: ENST00000414165.2:c.2349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2736C>T
  hgvsp: ENST00000342056.2:c.2736C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2679C>T
  hgvsp: ENST00000370398.1:c.2679C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2682C>T
  hgvsp: ENST00000355635.3:c.2682C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2652C>T
  hgvsp: ENST00000403813.2:c.2652C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2709C>T
  hgvsp: ENST00000402622.2:c.2709C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23059
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5501
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala912Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-73905029-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905029
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905029
    reference: chr 6
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2694C>G
  hgvsp: ENST00000355635.3:c.2694C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2664C>G
  hgvsp: ENST00000403813.2:c.2664C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2748C>G
  hgvsp: ENST00000342056.2:c.2748C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2361C>G
  hgvsp: ENST00000414165.2:c.2361C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2721C>G
  hgvsp: ENST00000402622.2:c.2721C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2691C>G
  hgvsp: ENST00000370398.1:c.2691C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2691C>G
  hgvsp: ENST00000355194.4:c.2691C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10156
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala916Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

6-73905034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905034
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905034
    reference: chr 6
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2696C>T
  hgvsp: ENSP00000359425.1:p.Ala899Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2366C>T
  hgvsp: ENSP00000409861.2:p.Ala789Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2699C>T
  hgvsp: ENSP00000347853.3:p.Ala900Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2726C>T
  hgvsp: ENSP00000385501.2:p.Ala909Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2669C>T
  hgvsp: ENSP00000384453.2:p.Ala890Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2696C>T
  hgvsp: ENSP00000347326.4:p.Ala899Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2753C>T
  hgvsp: ENSP00000345055.2:p.Ala918Val
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23021
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala918Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

6-73905040-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905040
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905040
    reference: chr 6
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2705A>T
  hgvsp: ENSP00000347853.3:p.Asp902Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2759A>T
  hgvsp: ENSP00000345055.2:p.Asp920Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2675A>T
  hgvsp: ENSP00000384453.2:p.Asp892Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2702A>T
  hgvsp: ENSP00000359425.1:p.Asp901Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2732A>T
  hgvsp: ENSP00000385501.2:p.Asp911Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2702A>T
  hgvsp: ENSP00000347326.4:p.Asp901Val
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2372A>T
  hgvsp: ENSP00000409861.2:p.Asp791Val
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp920Val
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

6-73905040-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905040
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905038
    reference: chr 6
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2737_2738delCT
  hgvsp: ENSP00000385501.2:p.Leu913LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2680_2681delCT
  hgvsp: ENSP00000384453.2:p.Leu894LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2377_2378delCT
  hgvsp: ENSP00000409861.2:p.Leu793LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2764_2765delCT
  hgvsp: ENSP00000345055.2:p.Leu922LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2710_2711delCT
  hgvsp: ENSP00000347853.3:p.Leu904LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2707_2708delCT
  hgvsp: ENSP00000359425.1:p.Leu903LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2707_2708delCT
  hgvsp: ENSP00000347326.4:p.Leu903LysfsTer13
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8120
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu922LysfsTer13
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: ACT
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-73905047-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905047
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905047
    reference: chr 6
allele count: 3
allele frequency: 2.476473501733531e-5
allele num: 121140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2712A>G
  hgvsp: ENST00000355635.3:c.2712A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2709A>G
  hgvsp: ENST00000370398.1:c.2709A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2709A>G
  hgvsp: ENST00000355194.4:c.2709A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2379A>G
  hgvsp: ENST00000414165.2:c.2379A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2682A>G
  hgvsp: ENST00000403813.2:c.2682A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2766A>G
  hgvsp: ENST00000342056.2:c.2766A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2739A>G
  hgvsp: ENST00000402622.2:c.2739A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu922Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

6-73905050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905050
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905050
    reference: chr 6
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2712G>A
  hgvsp: ENST00000370398.1:c.2712G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2712G>A
  hgvsp: ENST00000355194.4:c.2712G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2742G>A
  hgvsp: ENST00000402622.2:c.2742G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2382G>A
  hgvsp: ENST00000414165.2:c.2382G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2715G>A
  hgvsp: ENST00000355635.3:c.2715G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2769G>A
  hgvsp: ENST00000342056.2:c.2769G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2685G>A
  hgvsp: ENST00000403813.2:c.2685G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4214
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg923Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-73905055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905055
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905055
    reference: chr 6
allele count: 2
allele frequency: 1.651936896010573e-5
allele num: 121070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2690G>A
  hgvsp: ENSP00000384453.2:p.Gly897Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2387G>A
  hgvsp: ENSP00000409861.2:p.Gly796Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2717G>A
  hgvsp: ENSP00000359425.1:p.Gly906Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2747G>A
  hgvsp: ENSP00000385501.2:p.Gly916Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2720G>A
  hgvsp: ENSP00000347853.3:p.Gly907Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2774G>A
  hgvsp: ENSP00000345055.2:p.Gly925Glu
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2717G>A
  hgvsp: ENSP00000347326.4:p.Gly906Glu
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10163
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22745
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly925Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-73905059-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905059
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905059
    reference: chr 6
allele count: 22
allele frequency: 1.817941429232498e-4
allele num: 121016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2751G>T
  hgvsp: ENSP00000385501.2:p.Arg917Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2778G>T
  hgvsp: ENSP00000345055.2:p.Arg926Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2721G>T
  hgvsp: ENSP00000347326.4:p.Arg907Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2721G>T
  hgvsp: ENSP00000359425.1:p.Arg907Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2391G>T
  hgvsp: ENSP00000409861.2:p.Arg797Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2694G>T
  hgvsp: ENSP00000384453.2:p.Arg898Ser
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2724G>T
  hgvsp: ENSP00000347853.3:p.Arg908Ser
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10176
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 22727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg926Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-73905062-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905062
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905062
    reference: chr 6
allele count: 7
allele frequency: 5.786558650905183e-5
allele num: 120970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2394A>C
  hgvsp: ENST00000414165.2:c.2394A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2727A>C
  hgvsp: ENST00000355635.3:c.2727A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2781A>C
  hgvsp: ENST00000342056.2:c.2781A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2724A>C
  hgvsp: ENST00000355194.4:c.2724A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2754A>C
  hgvsp: ENST00000402622.2:c.2754A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2724A>C
  hgvsp: ENST00000370398.1:c.2724A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2697A>C
  hgvsp: ENST00000403813.2:c.2697A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22622
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser927Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

6-73905063-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905063
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905063
    reference: chr 6
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2782C>T
  hgvsp: ENSP00000345055.2:p.Arg928Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2725C>T
  hgvsp: ENSP00000347326.4:p.Arg909Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2755C>T
  hgvsp: ENSP00000385501.2:p.Arg919Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2725C>T
  hgvsp: ENSP00000359425.1:p.Arg909Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2728C>T
  hgvsp: ENSP00000347853.3:p.Arg910Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2698C>T
  hgvsp: ENSP00000384453.2:p.Arg900Ter
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2395C>T
  hgvsp: ENSP00000409861.2:p.Arg799Ter
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg928Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

6-73905064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905064
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905064
    reference: chr 6
allele count: 7
allele frequency: 5.788664141706498e-5
allele num: 120926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2756G>A
  hgvsp: ENSP00000385501.2:p.Arg919Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2783G>A
  hgvsp: ENSP00000345055.2:p.Arg928Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2699G>A
  hgvsp: ENSP00000384453.2:p.Arg900Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2396G>A
  hgvsp: ENSP00000409861.2:p.Arg799Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2726G>A
  hgvsp: ENSP00000359425.1:p.Arg909Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2726G>A
  hgvsp: ENSP00000347326.4:p.Arg909Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2729G>A
  hgvsp: ENSP00000347853.3:p.Arg910Gln
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4200
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5487
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg928Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-73905082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905082
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905082
    reference: chr 6
allele count: 2
allele frequency: 1.657797450307521e-5
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2747G>A
  hgvsp: ENSP00000347853.3:p.Cys916Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2744G>A
  hgvsp: ENSP00000359425.1:p.Cys915Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2774G>A
  hgvsp: ENSP00000385501.2:p.Cys925Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2717G>A
  hgvsp: ENSP00000384453.2:p.Cys906Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2414G>A
  hgvsp: ENSP00000409861.2:p.Cys805Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2744G>A
  hgvsp: ENSP00000347326.4:p.Cys915Tyr
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2801G>A
  hgvsp: ENSP00000345055.2:p.Cys934Tyr
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4185
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys934Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

6-73905083-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905083
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905083
    reference: chr 6
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2745T>C
  hgvsp: ENST00000370398.1:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2718T>C
  hgvsp: ENST00000403813.2:c.2718T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2775T>C
  hgvsp: ENST00000402622.2:c.2775T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2415T>C
  hgvsp: ENST00000414165.2:c.2415T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2748T>C
  hgvsp: ENST00000355635.3:c.2748T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2745T>C
  hgvsp: ENST00000355194.4:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2802T>C
  hgvsp: ENST00000342056.2:c.2802T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22390
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10177
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4291
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys934Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

6-73905086-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905086
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905086
    reference: chr 6
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2721G>A
  hgvsp: ENST00000403813.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2418G>A
  hgvsp: ENST00000414165.2:c.2418G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2778G>A
  hgvsp: ENST00000402622.2:c.2778G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2805G>A
  hgvsp: ENST00000342056.2:c.2805G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2748G>A
  hgvsp: ENST00000370398.1:c.2748G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2751G>A
  hgvsp: ENST00000355635.3:c.2751G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2748G>A
  hgvsp: ENST00000355194.4:c.2748G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys935Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-73905090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905090
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905090
    reference: chr 6
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2422G>A
  hgvsp: ENSP00000409861.2:p.Gly808Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2809G>A
  hgvsp: ENSP00000345055.2:p.Gly937Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2725G>A
  hgvsp: ENSP00000384453.2:p.Gly909Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2752G>A
  hgvsp: ENSP00000347326.4:p.Gly918Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2752G>A
  hgvsp: ENSP00000359425.1:p.Gly918Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2755G>A
  hgvsp: ENSP00000347853.3:p.Gly919Arg
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2782G>A
  hgvsp: ENSP00000385501.2:p.Gly928Arg
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10735
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly937Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

6-73905096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905096
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905096
    reference: chr 6
allele count: 1
allele frequency: 8.312413758707254e-6
allele num: 120302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2758A>G
  hgvsp: ENSP00000347326.4:p.Ser920Gly
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2428A>G
  hgvsp: ENSP00000409861.2:p.Ser810Gly
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2761A>G
  hgvsp: ENSP00000347853.3:p.Ser921Gly
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2731A>G
  hgvsp: ENSP00000384453.2:p.Ser911Gly
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2815A>G
  hgvsp: ENSP00000345055.2:p.Ser939Gly
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2758A>G
  hgvsp: ENSP00000359425.1:p.Ser920Gly
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2788A>G
  hgvsp: ENSP00000385501.2:p.Ser930Gly
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10179
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7938
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4285
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser939Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

6-73905116-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905116
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905116
    reference: chr 6
allele count: 1
allele frequency: 8.398844319021702e-6
allele num: 119064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2808G>T
  hgvsp: ENSP00000385501.2:p.Leu936Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2835G>T
  hgvsp: ENSP00000345055.2:p.Leu945Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2778G>T
  hgvsp: ENSP00000347326.4:p.Leu926Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2778G>T
  hgvsp: ENSP00000359425.1:p.Leu926Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2781G>T
  hgvsp: ENSP00000347853.3:p.Leu927Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2448G>T
  hgvsp: ENSP00000409861.2:p.Leu816Phe
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2751G>T
  hgvsp: ENSP00000384453.2:p.Leu917Phe
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10177
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu945Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-73905119-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905119
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905119
    reference: chr 6
allele count: 1
allele frequency: 8.411843876177658e-6
allele num: 118880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2754T>G
  hgvsp: ENST00000403813.2:c.2754T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2451T>G
  hgvsp: ENST00000414165.2:c.2451T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2781T>G
  hgvsp: ENST00000370398.1:c.2781T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2838T>G
  hgvsp: ENST00000342056.2:c.2838T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2811T>G
  hgvsp: ENST00000402622.2:c.2811T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2784T>G
  hgvsp: ENST00000355635.3:c.2784T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2781T>G
  hgvsp: ENST00000355194.4:c.2781T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21093
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro946Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-73905122-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905122
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905122
    reference: chr 6
allele count: 75
allele frequency: 6.326764745579701e-4
allele num: 118544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2787T>A
  hgvsp: ENSP00000347853.3:p.His929Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2841T>A
  hgvsp: ENSP00000345055.2:p.His947Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2454T>A
  hgvsp: ENSP00000409861.2:p.His818Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2784T>A
  hgvsp: ENSP00000347326.4:p.His928Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2814T>A
  hgvsp: ENSP00000385501.2:p.His938Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2784T>A
  hgvsp: ENSP00000359425.1:p.His928Gln
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2757T>A
  hgvsp: ENSP00000384453.2:p.His919Gln
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17237
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20870
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4121
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His947Gln
num of homozygotes: 2
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

6-73905134-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905134
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905134
    reference: chr 6
allele count: 1
allele frequency: 8.505860537910621e-6
allele num: 117566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.2796A>T
  hgvsp: ENSP00000359425.1:p.Lys932Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.2853A>T
  hgvsp: ENSP00000345055.2:p.Lys951Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347853
  ensembl transcript: ENST00000355635
  gene symbol: KCNQ5
  hgvsc: ENST00000355635.3:c.2799A>T
  hgvsp: ENSP00000347853.3:p.Lys933Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.2796A>T
  hgvsp: ENSP00000347326.4:p.Lys932Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000385501
  ensembl transcript: ENST00000402622
  gene symbol: KCNQ5
  hgvsc: ENST00000402622.2:c.2826A>T
  hgvsp: ENSP00000385501.2:p.Lys942Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000384453
  ensembl transcript: ENST00000403813
  gene symbol: KCNQ5
  hgvsc: ENST00000403813.2:c.2769A>T
  hgvsp: ENSP00000384453.2:p.Lys923Asn
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000409861
  ensembl transcript: ENST00000414165
  gene symbol: KCNQ5
  hgvsc: ENST00000414165.2:c.2466A>T
  hgvsp: ENSP00000409861.2:p.Lys822Asn
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7636
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4097
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys951Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

6-73905138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905138
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905138
    reference: chr 6
allele count: 4
allele frequency: 3.416350654231151e-5
allele num: 117084
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*1G>A
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*1G>A
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7620
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19732
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10225
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

6-73905148-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905148
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905148
    reference: chr 6
allele count: 1
allele frequency: 8.643640009680878e-6
allele num: 115692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*11T>C
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*11T>C
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*11T>C
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5367
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18280
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10225
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4060
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-73905151-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905151
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905151
    reference: chr 6
allele count: 2
allele frequency: 1.734424864714861e-5
allele num: 115312
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*14T>C
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*14T>C
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*14T>C
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10143
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4240
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4056
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17608
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10227
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

6-73905154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905154
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905154
    reference: chr 6
allele count: 1
allele frequency: 8.70412923891094e-6
allele num: 114888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*17C>T
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*17C>T
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5358
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4049
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10227
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

6-73905163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905163
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905163
    reference: chr 6
allele count: 14
allele frequency: 1.226370468999106e-4
allele num: 114158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*26G>A
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*26G>A
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*26G>A
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13520
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 10242
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 7214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16350
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

6-73905170-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905170
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905170
    reference: chr 6
allele count: 1
allele frequency: 8.799718409010911e-6
allele num: 113640
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*33T>G
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*33T>G
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*33T>G
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10238
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

6-73905174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905174
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905174
    reference: chr 6
allele count: 1
allele frequency: 8.83158173628897e-6
allele num: 113230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*37G>A
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10238
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5337
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/6-73905177-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73905177
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 73905177
    reference: chr 6
allele count: 1
allele frequency: 8.860064146864424e-6
allele num: 112866
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000345055
  ensembl transcript: ENST00000342056
  gene symbol: KCNQ5
  hgvsc: ENST00000342056.2:c.*40A>C
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000359425
  ensembl transcript: ENST00000370398
  gene symbol: KCNQ5
  hgvsc: ENST00000370398.1:c.*40A>C
  variant of: http://identifiers.org/hgnc/6299
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000185760
  ensembl protein: ENSP00000347326
  ensembl transcript: ENST00000355194
  gene symbol: KCNQ5
  hgvsc: ENST00000355194.4:c.*40A>C
  variant of: http://identifiers.org/hgnc/6299
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10256
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS

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

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

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

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

GenotypeQuality
all individuals: 4159
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4178
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10002
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e0

QD
type: SiteQuality
SIO_000300: 1.249e1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.49e0

DP
type: SiteQuality
SIO_000300: 1.874601e6

FS
type: SiteQuality
SIO_000300: 2.045e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.64e-1

MQ
type: SiteQuality
SIO_000300: 5.574e1

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

GenotypeQuality
all individuals: 4176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8167
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.874554e6

MQ
type: SiteQuality
SIO_000300: 5.992e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.964e0

QD
type: SiteQuality
SIO_000300: 1.519e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

FS
type: SiteQuality
SIO_000300: 2.789e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10004
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 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: 11546
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.371e1

FS
type: SiteQuality
SIO_000300: 1.2833e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: -7.299e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.763e0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.053e0

DP
type: SiteQuality
SIO_000300: 1.874109e6

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

GenotypeQuality
all individuals: 23547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
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: 908
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.786e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 1.882e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 1.87378e6

QD
type: SiteQuality
SIO_000300: 1.681e1

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 9.779999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.873625e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.743e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10004
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 6.485e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.167e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.001e0

DP
type: SiteQuality
SIO_000300: 1.873684e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.273e1

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

GenotypeQuality
all individuals: 2743
bin: 9.25e1
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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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 5387
bin: 7.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.237e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

FS
type: SiteQuality
SIO_000300: 1.005e1

VQSLOD
type: SiteQuality
SIO_000300: -3.845e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

DP
type: SiteQuality
SIO_000300: 1.873529e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e-1

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 23521
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

African
type: Population
allele count: 48
allele frequency: 4.614497212074601e-3
allele num: 10402
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: 16510
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

DP
type: SiteQuality
SIO_000300: 1.875711e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

QD
type: SiteQuality
SIO_000300: 1.445e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4150
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variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 4
allele frequency: 4.623208506703652e-4
allele num: 8652
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.873765e6

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

FS
type: SiteQuality
SIO_000300: 2.645e0

QD
type: SiteQuality
SIO_000300: 1.644e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e0

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

GenotypeQuality
all individuals: 4151
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10023
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variant carriers: 1

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.283e0

DP
type: SiteQuality
SIO_000300: 1.873747e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.271e1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.884e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
all individuals: 8134
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2750
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.028467595396729e-4
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.874134e6

FS
type: SiteQuality
SIO_000300: 4.037e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.335e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.801e1

DP
type: SiteQuality
SIO_000300: 1.87395e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.216e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 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: 6614
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.048e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.592e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.874545e6

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.494e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-2

GenotypeQuality
all individuals: 51
bin: 2.75e1
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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.922337562475971e-4
allele num: 10404
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
allele num: 908
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European (Non-Finnish)
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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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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 7.44e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.158e0

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

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

European (Non-Finnish)
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allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10404
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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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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Other
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allele num: 908
num of homozygotes: 0

African
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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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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.496807266840543e-5
allele num: 66714
num of homozygotes: 0

South Asian
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QD
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele num: 8648
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South Asian
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Other
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num of homozygotes: 0

VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.185e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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SIO_000300: 1.878008e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

Other
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Latino
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East Asian
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allele num: 8650
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European (Finnish)
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African
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South Asian
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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DP
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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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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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

Latino
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European (Finnish)
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African
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Other
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East Asian
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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African
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South Asian
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8654
num of homozygotes: 0

European (Finnish)
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Other
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European (Non-Finnish)
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African
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Latino
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South Asian
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DP
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 4.239854633555421e-4
allele num: 16510
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

Latino
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Other
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European (Finnish)
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African
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South Asian
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East Asian
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QD
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DP
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FS
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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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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European (Non-Finnish)
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South Asian
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allele num: 16510
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African
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Latino
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Other
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European (Finnish)
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East Asian
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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Other
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South Asian
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Latino
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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VQSLOD
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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allele num: 8652
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African
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Latino
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Other
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

South Asian
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allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.883395e6

MQ
type: SiteQuality
SIO_000300: 5.921e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

FS
type: SiteQuality
SIO_000300: 1.138e0

QD
type: SiteQuality
SIO_000300: 1.235e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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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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

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

FS
type: SiteQuality
SIO_000300: 4.628e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.109e1

DP
type: SiteQuality
SIO_000300: 1.883062e6

ReadPosRankSum
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SIO_000300: -1.226e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.559e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
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: 8654
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 9.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.305e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-1

DP
type: SiteQuality
SIO_000300: 1.883072e6

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 1.273e1

MQ
type: SiteQuality
SIO_000300: 6.099e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997781641585227e-5
allele num: 66716
num of homozygotes: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 11574
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: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.882973e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.533e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

QD
type: SiteQuality
SIO_000300: 1.246e1

FS
type: SiteQuality
SIO_000300: 4.194e0

VQSLOD
type: SiteQuality
SIO_000300: -1.272e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
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: 10398
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: 908
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.320027648176948e-4
allele num: 11574
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.802e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.883383e6

QD
type: SiteQuality
SIO_000300: 1.178e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 3.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
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: 10390
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.029201502483945e-4
allele num: 16506
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

DP
type: SiteQuality
SIO_000300: 1.883884e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.85e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.32e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

South Asian
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allele count: 5
allele frequency: 3.029201502483945e-4
allele num: 16506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.883884e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.118e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.32e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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: 66700
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

South Asian
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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: 11570
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.882389e6

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.818e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.647e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e0

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998770504093322e-5
allele num: 66694
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.88223e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.212e1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

FS
type: SiteQuality
SIO_000300: 4.098e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-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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bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
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
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num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.401e0

QD
type: SiteQuality
SIO_000300: 1.303e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.457e-1

DP
type: SiteQuality
SIO_000300: 1.882199e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e-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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variant carriers: 0

GenotypeQuality
all individuals: 10157
bin: 9.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
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: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

FS
type: SiteQuality
SIO_000300: 4.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

ClippingRankSum
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BaseQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.881721e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10382
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: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: -1.493e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.71e-1

QD
type: SiteQuality
SIO_000300: 1.074e1

VQSLOD
type: SiteQuality
SIO_000300: -1.685e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.706e0

DP
type: SiteQuality
SIO_000300: 1.880862e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.295e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 1.880551e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.25e1
variant carriers: 0

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.45e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

QD
type: SiteQuality
SIO_000300: 1.377e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

DP
type: SiteQuality
SIO_000300: 1.87981e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 22937
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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: 9.75e1
variant carriers: 2

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

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 1.87981e6

QD
type: SiteQuality
SIO_000300: 1.377e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.507753335737469e-5
allele num: 66552
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 7.181e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.97e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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
type: Population
allele count: 0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.140000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -6.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.159e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.936858415649816e-4
allele num: 10326
num of homozygotes: 0

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

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

Other
type: Population
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num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.531e1

MQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.02e-1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
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allele frequency: 9.699321047526673e-5
allele num: 10310
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.158939799632961e-4
allele num: 66478
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

BaseQRankSum
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SIO_000300: -3.077e0

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

GenotypeQuality
all individuals: 2250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10175
bin: 9.75e1
variant carriers: 7

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

DP
type: SiteQuality
SIO_000300: 1.875757e6

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.475e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22532
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10175
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 902
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.472e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 8.070000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.47e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

DP
type: SiteQuality
SIO_000300: 1.875175e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22449
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10182
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4294
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.52875986267542e-5
allele num: 66412
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.246e1

DP
type: SiteQuality
SIO_000300: 1.874925e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 1.119e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

GenotypeQuality
all individuals: 22382
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 694
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10177
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5483
bin: 7.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.019688368160406e-5
allele num: 66232
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 4.958e0

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.436e0

DP
type: SiteQuality
SIO_000300: 1.869261e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.001e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.386e1

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 704
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 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: 16500
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

DP
type: SiteQuality
SIO_000300: 1.869033e6

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 9.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.65e0

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

FS
type: SiteQuality
SIO_000300: 2.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

GenotypeQuality
all individuals: 7975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4291
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10177
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 753
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5476
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510847887834653e-5
allele num: 66188
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
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: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.083e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

FS
type: SiteQuality
SIO_000300: 1.798e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

QD
type: SiteQuality
SIO_000300: 1.23e1

DP
type: SiteQuality
SIO_000300: 1.868308e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

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

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22321
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10178
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4288
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 1.484e0

VQSLOD
type: SiteQuality
SIO_000300: -9.176e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.923e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.402e0

QD
type: SiteQuality
SIO_000300: 1.824e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

DP
type: SiteQuality
SIO_000300: 1.866628e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

GenotypeQuality
all individuals: 1047
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5467
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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: 1
allele frequency: 9.900990099009902e-5
allele num: 10100
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: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66014
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.86358e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

FS
type: SiteQuality
SIO_000300: 4.742e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.64e-1

QD
type: SiteQuality
SIO_000300: 1.081e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21206
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2788
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5436
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

FS
type: SiteQuality
SIO_000300: 1.611e0

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.032e0

DP
type: SiteQuality
SIO_000300: 1.844461e6

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
all individuals: 2033
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5433
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4136
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10177
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534118802160039e-5
allele num: 65184
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
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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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.19e-1

FS
type: SiteQuality
SIO_000300: 5.6369e1

InbreedingCoeff
type: SiteQuality
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MQ
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MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.841775e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-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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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 73

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

Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65010
num of homozygotes: 0

East Asian
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allele count: 75
allele frequency: 8.720930232558139e-3
allele num: 8600
num of homozygotes: 2

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
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BaseQRankSum
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QD
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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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64544
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.997e0

DP
type: SiteQuality
SIO_000300: 1.826591e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.17e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 4.667444574095683e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64330
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.057e1

FS
type: SiteQuality
SIO_000300: 2.568e0

ReadPosRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.819508e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.401e0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.568725880839582e-5
allele num: 63746
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: 0.0e0
allele num: 11472
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8970
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.839e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.793899e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 2.344116268166901e-4
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63598
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele num: 11470
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.16e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.784447e6

GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

Other
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African
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 15110
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 63100
num of homozygotes: 0

Latino
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allele frequency: 8.732099196646873e-5
allele num: 11452
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Other
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East Asian
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South Asian
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African
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allele frequency: 1.481650330521997e-3
allele num: 8774
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.589622941438291e-5
allele num: 62908
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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Other
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

African
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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South Asian
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Other
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European (Finnish)
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East Asian
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QD
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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DP
type: SiteQuality
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FS
type: SiteQuality
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