http://identifiers.org/exac.variant/5-122923884-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122923884
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122923884
    reference: chr 5
allele count: 1
allele frequency: 8.364421098415779e-6
allele num: 119554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.534+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.420+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.759+37A>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

5-122924073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924073
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924073
    reference: chr 5
allele count: 5
allele frequency: 4.216278206901204e-5
allele num: 118588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-48A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-48A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12726
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3066
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3986
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

5-122924074-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924074
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924073
    reference: chr 5
allele count: 1
allele frequency: 8.442380751371886e-6
allele num: 118450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-45delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-45delA
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3026
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7889
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: TA
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

5-122924075-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924075
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924075
    reference: chr 5
allele count: 1
allele frequency: 8.436825053995681e-6
allele num: 118528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-46A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-46A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3133
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

5-122924076-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924076
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924076
    reference: chr 5
allele count: 1
allele frequency: 8.438391305081599e-6
allele num: 118506
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-45A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10646
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7984
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

5-122924082-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924082
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924082
    reference: chr 5
allele count: 1
allele frequency: 8.418075291265404e-6
allele num: 118792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-39A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

5-122924087-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924087
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924087
    reference: chr 5
allele count: 1
allele frequency: 8.400537634408602e-6
allele num: 119040
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-34A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8310
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/5-122924088-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924088
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924088
    reference: chr 5
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-33C>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-122924088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924088
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924088
    reference: chr 5
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-33C>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-33C>T
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

5-122924090-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924090
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924090
    reference: chr 5
allele count: 9
allele frequency: 7.548435796359976e-5
allele num: 119230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-31A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11110
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7920
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

5-122924098-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924098
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924098
    reference: chr 5
allele count: 1
allele frequency: 8.354777261638205e-6
allele num: 119692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-23A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-23A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

5-122924101-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924101
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924102
    reference: chr 5
allele count: 140
allele frequency: 1.300680069865101e-3
allele num: 107636
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-10dupT
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 3.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 3.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 2.5e0
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22190
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 5.25e1
  variant carriers: 4
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

5-122924101-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924101
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924101
    reference: chr 5
allele count: 2
allele frequency: 1.858114385521573e-5
allele num: 107636
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4966
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 2
  allele frequency: 3.391094984570518e-5
  allele num: 58978
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8846
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 836
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 14732
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

5-122924101-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924101
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924100
    reference: chr 5
allele count: 688
allele frequency: 6.39191348619421e-3
allele num: 107636
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-10delT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-10delT
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 6.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 5.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 3.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 5.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 283
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 5.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 7.5e0
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 8.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 12
num of homozygotes: 1
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: AT
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

5-122924105-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924105
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924105
    reference: chr 5
allele count: 14
allele frequency: 1.16398949083774e-4
allele num: 120276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.421-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.760-16T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.535-16T>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13363
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 33521
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

5-122924138-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924138
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924138
    reference: chr 5
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.777G>C
  hgvsp: ENSP00000354942.2:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.777G>C
  hgvsp: ENSP00000334735.4:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.777G>C
  hgvsp: ENSP00000429412.1:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.777G>C
  hgvsp: ENSP00000353904.2:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.552G>C
  hgvsp: ENSP00000421998.3:p.Glu184Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.438G>C
  hgvsp: ENSP00000421385.2:p.Glu146Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.20G>C
  hgvsp: ENSP00000429914.1:p.Glu7Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.777G>C
  hgvsp: ENSP00000378807.1:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.777G>C
  hgvsp: ENSP00000378806.1:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.777G>C
  hgvsp: ENSP00000423838.2:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu259Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

5-122924172-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924172
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924172
    reference: chr 5
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.811A>T
  hgvsp: ENSP00000429412.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.472A>T
  hgvsp: ENSP00000421385.2:p.Thr158Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.811A>T
  hgvsp: ENSP00000423838.2:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.811A>T
  hgvsp: ENSP00000378806.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.811A>T
  hgvsp: ENSP00000353904.2:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.586A>T
  hgvsp: ENSP00000421998.3:p.Thr196Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.54A>T
  hgvsp: ENSP00000429914.1:p.Thr19Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.811A>T
  hgvsp: ENSP00000334735.4:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.811A>T
  hgvsp: ENSP00000354942.2:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.811A>T
  hgvsp: ENSP00000378807.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr271Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

5-122924178-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924178
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924178
    reference: chr 5
allele count: 5
allele frequency: 4.128546421375962e-5
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.817A>G
  hgvsp: ENSP00000429412.1:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.60A>G
  hgvsp: ENSP00000429914.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.817A>G
  hgvsp: ENSP00000423838.2:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.817A>G
  hgvsp: ENSP00000354942.2:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.817A>G
  hgvsp: ENSP00000353904.2:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.817A>G
  hgvsp: ENSP00000378807.1:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.478A>G
  hgvsp: ENSP00000421385.2:p.Ile160Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.592A>G
  hgvsp: ENSP00000421998.3:p.Ile198Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.817A>G
  hgvsp: ENSP00000334735.4:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.817A>G
  hgvsp: ENSP00000378806.1:p.Ile273Val
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile273Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

5-122924193-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924193
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924193
    reference: chr 5
allele count: 3
allele frequency: 2.479461791493793e-5
allele num: 120994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.832G>C
  hgvsp: ENSP00000423838.2:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.832G>C
  hgvsp: ENSP00000429412.1:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.832G>C
  hgvsp: ENSP00000354942.2:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.75G>C
  hgvsp: ENSP00000429914.1:p.Glu26Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.832G>C
  hgvsp: ENSP00000353904.2:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.607G>C
  hgvsp: ENSP00000421998.3:p.Glu203Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.832G>C
  hgvsp: ENSP00000334735.4:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.493G>C
  hgvsp: ENSP00000421385.2:p.Glu165Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.832G>C
  hgvsp: ENSP00000378806.1:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.832G>C
  hgvsp: ENSP00000378807.1:p.Glu278Gln
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3377
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu278Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

5-122924205-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924205
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924205
    reference: chr 5
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505G>C
  hgvsp: ENSP00000421385.2:p.Glu169Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844G>C
  hgvsp: ENSP00000423838.2:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619G>C
  hgvsp: ENSP00000421998.3:p.Glu207Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844G>C
  hgvsp: ENSP00000354942.2:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844G>C
  hgvsp: ENSP00000429412.1:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87G>C
  hgvsp: ENSP00000429914.1:p.Glu30Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844G>C
  hgvsp: ENSP00000353904.2:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844G>C
  hgvsp: ENSP00000334735.4:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844G>C
  hgvsp: ENSP00000378807.1:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844G>C
  hgvsp: ENSP00000378806.1:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu282Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

5-122924229-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924229
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924229
    reference: chr 5
allele count: 6
allele frequency: 5.01898850651632e-5
allele num: 119546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+24A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+24A>T
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21068
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10390
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-122924230-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924230
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924230
    reference: chr 5
allele count: 1
allele frequency: 8.369321415419637e-6
allele num: 119484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+25C>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+25C>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3209
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

5-122924231-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924231
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924231
    reference: chr 5
allele count: 6
allele frequency: 5.019240421616196e-5
allele num: 119540
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+26A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+26A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21116
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

5-122924233-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924233
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924233
    reference: chr 5
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+28T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+28T>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12081
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28990
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

5-122924241-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924241
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924241
    reference: chr 5
allele count: 2
allele frequency: 1.686454398273071e-5
allele num: 118592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+36G>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

5-122924245-A-AAAAAAAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924245
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924252
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 118356
alternate allele: AAAAAAAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+40_619+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+40_87+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+40_844+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+40_505+41insAAAAAAT
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3863
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-122924257-A-AATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122924257
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122924260
    reference: chr 5
allele count: 1
allele frequency: 8.661308203991131e-6
allele num: 115456
alternate allele: AATT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.87+53_87+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.619+53_619+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.505+53_505+55dupATT
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.844+53_844+55dupATT
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5099
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5003
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

5-122926055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926055
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926055
    reference: chr 5
allele count: 1
allele frequency: 1.661295145695584e-5
allele num: 60194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.620-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.845-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.845-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.845-49T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.845-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.845-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.845-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.506-49T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.845-52T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.88-49T>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14003
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5837
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4207
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

5-122926062-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926062
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926062
    reference: chr 5
allele count: 1
allele frequency: 1.649892756970797e-5
allele num: 60610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.506-42T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.620-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.88-42T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.845-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.845-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.845-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.845-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.845-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.845-45T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.845-42T>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13707
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8056
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

5-122926062-TAAAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926062
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926057
    reference: chr 5
allele count: 1
allele frequency: 1.649892756970797e-5
allele num: 60610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.845-40_845-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.845-37_845-33delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.620-40_620-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.845-40_845-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.845-40_845-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.845-40_845-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.506-37_506-33delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.845-40_845-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.88-37_88-33delAAAAG
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.845-40_845-36delAAAAG
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6041
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 2.5e0
  variant carriers: 0
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: TAAAGA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

5-122926066-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926066
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926066
    reference: chr 5
allele count: 1
allele frequency: 1.638431038437592e-5
allele num: 61034
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.88-38G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.845-38G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.845-41G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.506-38G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.845-41G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.845-41G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.620-41G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.845-41G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.845-41G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.845-41G>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16007
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

5-122926067-AAAAGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926067
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926062
    reference: chr 5
allele count: 2
allele frequency: 3.256692503093858e-5
allele num: 61412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.88-35_88-31delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.845-38_845-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.620-38_620-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.845-38_845-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.845-38_845-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.845-38_845-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.506-35_506-31delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.845-38_845-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.845-38_845-34delAAGTA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.845-35_845-31delAAGTA
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13426
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: AAAAGT
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

5-122926073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926073
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926073
    reference: chr 5
allele count: 6
allele frequency: 9.545931842046648e-5
allele num: 62854
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.845-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.845-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.845-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.845-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.845-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.620-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.88-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.506-31A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.845-34A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.845-34A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20399
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11959
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

5-122926117-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926117
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926117
    reference: chr 5
allele count: 1
allele frequency: 9.045844339110612e-6
allele num: 110548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.630A>G
  hgvsp: ENST00000512718.3:c.630A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.855A>G
  hgvsp: ENST00000361991.2:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.855A>G
  hgvsp: ENST00000345990.4:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.855A>G
  hgvsp: ENST00000360683.2:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.858A>G
  hgvsp: ENST00000510842.2:c.858A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.855A>G
  hgvsp: ENST00000395412.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.855A>G
  hgvsp: ENST00000521364.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.855A>G
  hgvsp: ENST00000395411.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.101A>G
  hgvsp: ENST00000515322.2:c.101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.519A>G
  hgvsp: ENST00000511130.2:c.519A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr285Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-122926121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926121
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926121
    reference: chr 5
allele count: 1
allele frequency: 8.912973724553461e-6
allele num: 112196
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.859C>T
  hgvsp: ENSP00000378807.1:p.Leu287Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.105C>T
  hgvsp: ENSP00000429914.1:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.859C>T
  hgvsp: ENSP00000334735.4:p.Leu287Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.523C>T
  hgvsp: ENSP00000421385.2:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.634C>T
  hgvsp: ENSP00000421998.3:p.Leu212Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.859C>T
  hgvsp: ENSP00000378806.1:p.Leu287Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.862C>T
  hgvsp: ENSP00000423838.2:p.Leu288Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.859C>T
  hgvsp: ENSP00000429412.1:p.Leu287Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.859C>T
  hgvsp: ENSP00000354942.2:p.Leu287Phe
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.859C>T
  hgvsp: ENSP00000353904.2:p.Leu287Phe
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu287Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

5-122926125-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926125
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926125
    reference: chr 5
allele count: 3
allele frequency: 2.628811777076761e-5
allele num: 114120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.863G>A
  hgvsp: ENSP00000334735.4:p.Arg288His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.638G>A
  hgvsp: ENSP00000421998.3:p.Arg213His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.863G>A
  hgvsp: ENSP00000378806.1:p.Arg288His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.863G>A
  hgvsp: ENSP00000353904.2:p.Arg288His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.863G>A
  hgvsp: ENSP00000378807.1:p.Arg288His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.863G>A
  hgvsp: ENSP00000354942.2:p.Arg288His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.109G>A
  hgvsp: ENSP00000429914.1:p.Arg37His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.863G>A
  hgvsp: ENSP00000429412.1:p.Arg288His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.527G>A
  hgvsp: ENSP00000421385.2:p.Arg176His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.866G>A
  hgvsp: ENSP00000423838.2:p.Arg289His
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5001
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg288His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

5-122926129-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926129
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926129
    reference: chr 5
allele count: 3
allele frequency: 2.595200609007076e-5
allele num: 115598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.642T>C
  hgvsp: ENST00000512718.3:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.113T>C
  hgvsp: ENST00000515322.2:c.113T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.867T>C
  hgvsp: ENST00000521364.1:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.867T>C
  hgvsp: ENST00000361991.2:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.867T>C
  hgvsp: ENST00000395411.1:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.867T>C
  hgvsp: ENST00000345990.4:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.867T>C
  hgvsp: ENST00000360683.2:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.531T>C
  hgvsp: ENST00000511130.2:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.867T>C
  hgvsp: ENST00000395412.1:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.870T>C
  hgvsp: ENST00000510842.2:c.870T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr289Tyr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

5-122926138-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926138
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926138
    reference: chr 5
allele count: 1
allele frequency: 8.507018290089324e-6
allele num: 117550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.876G>T
  hgvsp: ENSP00000353904.2:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.876G>T
  hgvsp: ENSP00000378806.1:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.876G>T
  hgvsp: ENSP00000354942.2:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.651G>T
  hgvsp: ENSP00000421998.3:p.Arg217Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.122G>T
  hgvsp: ENSP00000429914.1:p.Arg41Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.876G>T
  hgvsp: ENSP00000429412.1:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.879G>T
  hgvsp: ENSP00000423838.2:p.Arg293Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.540G>T
  hgvsp: ENSP00000421385.2:p.Arg180Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.876G>T
  hgvsp: ENSP00000334735.4:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.876G>T
  hgvsp: ENSP00000378807.1:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg292Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

5-122926139-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926139
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926139
    reference: chr 5
allele count: 1
allele frequency: 8.496465470364328e-6
allele num: 117696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.877C>G
  hgvsp: ENSP00000334735.4:p.Leu293Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.877C>G
  hgvsp: ENSP00000354942.2:p.Leu293Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.877C>G
  hgvsp: ENSP00000353904.2:p.Leu293Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.123C>G
  hgvsp: ENSP00000429914.1:p.Leu42Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.877C>G
  hgvsp: ENSP00000378807.1:p.Leu293Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.652C>G
  hgvsp: ENSP00000421998.3:p.Leu218Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.877C>G
  hgvsp: ENSP00000378806.1:p.Leu293Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.541C>G
  hgvsp: ENSP00000421385.2:p.Leu181Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.877C>G
  hgvsp: ENSP00000429412.1:p.Leu293Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.880C>G
  hgvsp: ENSP00000423838.2:p.Leu294Val
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu293Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

5-122926164-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926164
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926164
    reference: chr 5
allele count: 1
allele frequency: 8.368200836820084e-6
allele num: 119500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.677A>G
  hgvsp: ENSP00000421998.3:p.Tyr226Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.902A>G
  hgvsp: ENSP00000354942.2:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.902A>G
  hgvsp: ENSP00000378806.1:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.902A>G
  hgvsp: ENSP00000334735.4:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.905A>G
  hgvsp: ENSP00000423838.2:p.Tyr302Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.902A>G
  hgvsp: ENSP00000353904.2:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.148A>G
  hgvsp: ENSP00000429914.1:p.Tyr50Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.902A>G
  hgvsp: ENSP00000378807.1:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.902A>G
  hgvsp: ENSP00000429412.1:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.566A>G
  hgvsp: ENSP00000421385.2:p.Tyr189Cys
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr301Cys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-122926180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926180
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926180
    reference: chr 5
allele count: 1
allele frequency: 8.336112037345782e-6
allele num: 119960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.918G>A
  hgvsp: ENST00000521364.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.918G>A
  hgvsp: ENST00000345990.4:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.693G>A
  hgvsp: ENST00000512718.3:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.918G>A
  hgvsp: ENST00000395411.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.918G>A
  hgvsp: ENST00000360683.2:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.921G>A
  hgvsp: ENST00000510842.2:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.164G>A
  hgvsp: ENST00000515322.2:c.164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.918G>A
  hgvsp: ENST00000395412.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.918G>A
  hgvsp: ENST00000361991.2:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.582G>A
  hgvsp: ENST00000511130.2:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys306Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

5-122926187-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926187
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926187
    reference: chr 5
allele count: 15
allele frequency: 1.248481014765369e-4
allele num: 120146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.925A>G
  hgvsp: ENSP00000334735.4:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.928A>G
  hgvsp: ENSP00000423838.2:p.Thr310Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.171A>G
  hgvsp: ENSP00000429914.1:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.925A>G
  hgvsp: ENSP00000353904.2:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.925A>G
  hgvsp: ENSP00000378806.1:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.925A>G
  hgvsp: ENSP00000354942.2:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.700A>G
  hgvsp: ENSP00000421998.3:p.Thr234Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.925A>G
  hgvsp: ENSP00000429412.1:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.925A>G
  hgvsp: ENSP00000378807.1:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.589A>G
  hgvsp: ENSP00000421385.2:p.Thr197Ala
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 9.75e1
  variant carriers: 14
hgvs: p.Thr309Ala
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

5-122926197-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926197
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926197
    reference: chr 5
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.181T>A
  hgvsp: ENSP00000429914.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.935T>A
  hgvsp: ENSP00000429412.1:p.Phe312Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.935T>A
  hgvsp: ENSP00000334735.4:p.Phe312Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.710T>A
  hgvsp: ENSP00000421998.3:p.Phe237Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.935T>A
  hgvsp: ENSP00000378807.1:p.Phe312Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.935T>A
  hgvsp: ENSP00000353904.2:p.Phe312Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.599T>A
  hgvsp: ENSP00000421385.2:p.Phe200Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.935T>A
  hgvsp: ENSP00000354942.2:p.Phe312Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.935T>A
  hgvsp: ENSP00000378806.1:p.Phe312Tyr
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.938T>A
  hgvsp: ENSP00000423838.2:p.Phe313Tyr
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe312Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

5-122926203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926203
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926203
    reference: chr 5
allele count: 2
allele frequency: 1.66306336271412e-5
allele num: 120260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.941G>A
  hgvsp: ENSP00000378806.1:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.716G>A
  hgvsp: ENSP00000421998.3:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.941G>A
  hgvsp: ENSP00000429412.1:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.941G>A
  hgvsp: ENSP00000353904.2:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.944G>A
  hgvsp: ENSP00000423838.2:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.605G>A
  hgvsp: ENSP00000421385.2:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.187G>A
  hgvsp: ENSP00000429914.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.941G>A
  hgvsp: ENSP00000334735.4:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.941G>A
  hgvsp: ENSP00000378807.1:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.941G>A
  hgvsp: ENSP00000354942.2:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg314Gln
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-122926210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926210
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926210
    reference: chr 5
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.951A>G
  hgvsp: ENST00000510842.2:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.948A>G
  hgvsp: ENST00000395412.1:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.948A>G
  hgvsp: ENST00000521364.1:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.948A>G
  hgvsp: ENST00000395411.1:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.948A>G
  hgvsp: ENST00000345990.4:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.948A>G
  hgvsp: ENST00000361991.2:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.194A>G
  hgvsp: ENST00000515322.2:c.194A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.612A>G
  hgvsp: ENST00000511130.2:c.612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.948A>G
  hgvsp: ENST00000360683.2:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.723A>G
  hgvsp: ENST00000512718.3:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly316Gly
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: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

5-122926212-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926212
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926212
    reference: chr 5
allele count: 2
allele frequency: 1.66267624368183e-5
allele num: 120288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.953A>G
  hgvsp: ENSP00000423838.2:p.Tyr318Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.725A>G
  hgvsp: ENSP00000421998.3:p.Tyr242Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.950A>G
  hgvsp: ENSP00000353904.2:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.950A>G
  hgvsp: ENSP00000429412.1:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.196A>G
  hgvsp: ENSP00000429914.1:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.614A>G
  hgvsp: ENSP00000421385.2:p.Tyr205Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.950A>G
  hgvsp: ENSP00000354942.2:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.950A>G
  hgvsp: ENSP00000378806.1:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.950A>G
  hgvsp: ENSP00000334735.4:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.950A>G
  hgvsp: ENSP00000378807.1:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr317Cys
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

5-122926214-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926214
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926214
    reference: chr 5
allele count: 1
allele frequency: 8.314763694415805e-6
allele num: 120268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.952A>G
  hgvsp: ENSP00000334735.4:p.Met318Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.952A>G
  hgvsp: ENSP00000429412.1:p.Met318Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.955A>G
  hgvsp: ENSP00000423838.2:p.Met319Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.952A>G
  hgvsp: ENSP00000354942.2:p.Met318Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.952A>G
  hgvsp: ENSP00000378806.1:p.Met318Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.952A>G
  hgvsp: ENSP00000353904.2:p.Met318Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.616A>G
  hgvsp: ENSP00000421385.2:p.Met206Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.727A>G
  hgvsp: ENSP00000421998.3:p.Met243Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.198A>G
  hgvsp: ENSP00000429914.1:p.Met67Val
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.952A>G
  hgvsp: ENSP00000378807.1:p.Met318Val
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1911
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met318Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/5-122926234-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926234
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926234
    reference: chr 5
allele count: 1
allele frequency: 8.325840077263796e-6
allele num: 120108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.218C>A
  hgvsp: ENSP00000429914.1:p.Asp73Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.972C>A
  hgvsp: ENSP00000378806.1:p.Asp324Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.972C>A
  hgvsp: ENSP00000353904.2:p.Asp324Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.972C>A
  hgvsp: ENSP00000429412.1:p.Asp324Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.747C>A
  hgvsp: ENSP00000421998.3:p.Asp249Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.972C>A
  hgvsp: ENSP00000334735.4:p.Asp324Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.636C>A
  hgvsp: ENSP00000421385.2:p.Asp212Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.972C>A
  hgvsp: ENSP00000354942.2:p.Asp324Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.975C>A
  hgvsp: ENSP00000423838.2:p.Asp325Glu
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.972C>A
  hgvsp: ENSP00000378807.1:p.Asp324Glu
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45786
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp324Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

5-122926259-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926259
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926259
    reference: chr 5
allele count: 1
allele frequency: 8.462241478522831e-6
allele num: 118172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+7A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+7A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43876
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 0
hgvs: c.990+7A>G
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

5-122926266-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926266
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926266
    reference: chr 5
allele count: 1
allele frequency: 8.499498529586754e-6
allele num: 117654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+14A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+14A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

5-122926276-ATTAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926276
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926272
    reference: chr 5
allele count: 19
allele frequency: 1.619253779679217e-4
allele num: 117338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+29_990+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+29_993+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+29_990+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+29_990+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+29_990+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+29_990+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+29_765+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+29_236+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+29_654+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+29_990+32delTTAC
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42728
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: ATTAC
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

5-122926284-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926284
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926284
    reference: chr 5
allele count: 1
allele frequency: 8.539417953272305e-6
allele num: 117104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+32C>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+32C>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

5-122926285-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926285
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926285
    reference: chr 5
allele count: 1
allele frequency: 8.541022531217438e-6
allele num: 117082
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+33A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+33A>T
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41168
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

5-122926292-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926292
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926292
    reference: chr 5
allele count: 5
allele frequency: 4.282655246252677e-5
allele num: 116750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+40G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+40G>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

5-122926293-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926293
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926293
    reference: chr 5
allele count: 4
allele frequency: 3.427357164890153e-5
allele num: 116708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+41T>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+41T>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

5-122926295-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926295
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926295
    reference: chr 5
allele count: 1
allele frequency: 8.575888033205839e-6
allele num: 116606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.990+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.654+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.990+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.990+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.990+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.765+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.990+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.990+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.236+43G>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.993+43G>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

5-122926967-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926967
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926967
    reference: chr 5
allele count: 1
allele frequency: 1.033143234978097e-5
allele num: 96792
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-46A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-46A>T
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7171
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

5-122926981-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926981
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926981
    reference: chr 5
allele count: 1
allele frequency: 9.868550901985552e-6
allele num: 101332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-32A>T
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-32A>T
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

5-122926983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926983
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926983
    reference: chr 5
allele count: 93
allele frequency: 9.076890042749224e-4
allele num: 102458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-30G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-30G>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 30208
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3766
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

5-122926985-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926985
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926985
    reference: chr 5
allele count: 1
allele frequency: 9.638368416994371e-6
allele num: 103752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-28A>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-28A>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31840
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32653
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8084
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-122926987-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926987
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926987
    reference: chr 5
allele count: 1
allele frequency: 9.516739945564248e-6
allele num: 105078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-26T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-26T>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-122926988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926988
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926988
    reference: chr 5
allele count: 3
allele frequency: 2.83967211252674e-5
allele num: 105646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-25G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-25G>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3709
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7311
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/5-122926993-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926993
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926992
    reference: chr 5
allele count: 1
allele frequency: 9.178185289204618e-6
allele num: 108954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-18delA
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-18delA
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: CA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

5-122926999-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122926999
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122926999
    reference: chr 5
allele count: 1
allele frequency: 8.917424647761727e-6
allele num: 112140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-14T>G
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-14T>G
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39971
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

5-122927002-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122927002
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122927002
    reference: chr 5
allele count: 6
allele frequency: 5.295301302644121e-5
allele num: 113308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-11T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-11T>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

5-122927004-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122927004
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122927004
    reference: chr 5
allele count: 1
allele frequency: 8.770852702299717e-6
allele num: 114014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-9G>A
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-9G>A
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41210
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

5-122927008-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122927008
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122927008
    reference: chr 5
allele count: 84
allele frequency: 7.279660282520149e-4
allele num: 115390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.991-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.766-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.991-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.237-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.991-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.994-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.991-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.991-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.991-5T>C
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.655-5T>C
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42003
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 2.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 2.25e1
  variant carriers: 0
hgvs: c.991-5T>C
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/5-122927014-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122927014
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122927014
    reference: chr 5
allele count: 1
allele frequency: 8.553880895762407e-6
allele num: 116906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.767C>A
  hgvsp: ENSP00000421998.3:p.Pro256His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.992C>A
  hgvsp: ENSP00000353904.2:p.Pro331His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.992C>A
  hgvsp: ENSP00000378806.1:p.Pro331His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.995C>A
  hgvsp: ENSP00000423838.2:p.Pro332His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.992C>A
  hgvsp: ENSP00000334735.4:p.Pro331His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.992C>A
  hgvsp: ENSP00000429412.1:p.Pro331His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.992C>A
  hgvsp: ENSP00000378807.1:p.Pro331His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.992C>A
  hgvsp: ENSP00000354942.2:p.Pro331His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.238C>A
  hgvsp: ENSP00000429914.1:p.Pro80His
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.656C>A
  hgvsp: ENSP00000421385.2:p.Pro219His
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro331His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

5-122927016-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122927016
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 122927016
    reference: chr 5
allele count: 1
allele frequency: 8.521226374899876e-6
allele num: 117354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421998
  ensembl transcript: ENST00000512718
  gene symbol: CSNK1G3
  hgvsc: ENST00000512718.3:c.769A>G
  hgvsp: ENSP00000421998.3:p.Thr257Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000334735
  ensembl transcript: ENST00000345990
  gene symbol: CSNK1G3
  hgvsc: ENST00000345990.4:c.994A>G
  hgvsp: ENSP00000334735.4:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429412
  ensembl transcript: ENST00000521364
  gene symbol: CSNK1G3
  hgvsc: ENST00000521364.1:c.994A>G
  hgvsp: ENSP00000429412.1:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000353904
  ensembl transcript: ENST00000360683
  gene symbol: CSNK1G3
  hgvsc: ENST00000360683.2:c.994A>G
  hgvsp: ENSP00000353904.2:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000354942
  ensembl transcript: ENST00000361991
  gene symbol: CSNK1G3
  hgvsc: ENST00000361991.2:c.994A>G
  hgvsp: ENSP00000354942.2:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000423838
  ensembl transcript: ENST00000510842
  gene symbol: CSNK1G3
  hgvsc: ENST00000510842.2:c.997A>G
  hgvsp: ENSP00000423838.2:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378807
  ensembl transcript: ENST00000395412
  gene symbol: CSNK1G3
  hgvsc: ENST00000395412.1:c.994A>G
  hgvsp: ENSP00000378807.1:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000421385
  ensembl transcript: ENST00000511130
  gene symbol: CSNK1G3
  hgvsc: ENST00000511130.2:c.658A>G
  hgvsp: ENSP00000421385.2:p.Thr220Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000378806
  ensembl transcript: ENST00000395411
  gene symbol: CSNK1G3
  hgvsc: ENST00000395411.1:c.994A>G
  hgvsp: ENSP00000378806.1:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/2456
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151292
  ensembl protein: ENSP00000429914
  ensembl transcript: ENST00000515322
  gene symbol: CSNK1G3
  hgvsc: ENST00000515322.2:c.240A>G
  hgvsp: ENSP00000429914.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/2456
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr332Ala
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
reference allele: A

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2728
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19854
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 217
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3999
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5557
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65780
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.177856301531213e-4
allele num: 8490
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.086e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.294e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.22e0

DP
type: SiteQuality
SIO_000300: 2.213848e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.036e0

MQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 7900
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 239
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 4
allele frequency: 3.520506953001232e-4
allele num: 11362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529145513487063e-5
allele num: 65396
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.835435e6

QD
type: SiteQuality
SIO_000300: 1.51e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

GenotypeQuality
all individuals: 230
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22492
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3907
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

FS
type: SiteQuality
SIO_000300: 2.619e0

MQ
type: SiteQuality
SIO_000300: 5.997e1

DP
type: SiteQuality
SIO_000300: 1.839887e6

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

QD
type: SiteQuality
SIO_000300: 1.846e1

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7886
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7972
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.210067763794773e-4
allele num: 8264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

FS
type: SiteQuality
SIO_000300: 6.997e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

QD
type: SiteQuality
SIO_000300: 1.566e1

VQSLOD
type: SiteQuality
SIO_000300: 4.58e-1

DP
type: SiteQuality
SIO_000300: 1.843693e6

GenotypeQuality
all individuals: 1037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1929
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7887
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23518
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.034554107179805e-4
allele num: 9666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65342
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.755e0

DP
type: SiteQuality
SIO_000300: 1.848142e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

GenotypeQuality
all individuals: 3996
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7902
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25545
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.865226e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

FS
type: SiteQuality
SIO_000300: 3.245e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7907
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27014
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4043
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523136442562525e-5
allele num: 65654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

DP
type: SiteQuality
SIO_000300: 1.879985e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.45e-1

QD
type: SiteQuality
SIO_000300: 3.322e1

GenotypeQuality
all individuals: 380
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7906
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4031
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65686
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

DP
type: SiteQuality
SIO_000300: 1.882894e6

QD
type: SiteQuality
SIO_000300: 1.045e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.832e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeQuality
all individuals: 3100
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4031
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7906
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65686
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.028383381324558e-4
allele num: 9724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

MQ
type: SiteQuality
SIO_000300: 5.908e1

QD
type: SiteQuality
SIO_000300: 1.045e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.832e0

DP
type: SiteQuality
SIO_000300: 1.882894e6

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8391
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variant carriers: 0

GenotypeQuality
all individuals: 4093
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variant carriers: 0

GenotypeQuality
all individuals: 174
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variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

GenotypeQuality
all individuals: 3253
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 121
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variant carriers: 0

GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 27552
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variant carriers: 0

GenotypeQuality
all individuals: 352
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variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.368405047894177e-4
allele num: 65770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.888395e6

FS
type: SiteQuality
SIO_000300: 1.063e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.28e1

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
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variant carriers: 0

GenotypeQuality
all individuals: 7919
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3301
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3138
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.182592242194891e-4
allele num: 8456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66018
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 1.902736e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.641e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.33e0

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1534
bin: 4.25e1
variant carriers: 10

GenotypeQuality
all individuals: 4966
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 1068
bin: 7.5e0
variant carriers: 38

GenotypeQuality
all individuals: 1255
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1439
bin: 3.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1462
bin: 3.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2553
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1815
bin: 2.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1002
bin: 1.75e1
variant carriers: 29

GenotypeQuality
all individuals: 964
bin: 1.25e1
variant carriers: 22

GenotypeQuality
all individuals: 6231
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1193
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1474
bin: 2.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1885
bin: 8.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.469590775491748e-3
allele num: 8846
num of homozygotes: 0

East Asian
type: Population
allele count: 47
allele frequency: 6.099143524526343e-3
allele num: 7706
num of homozygotes: 0

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

South Asian
type: Population
allele count: 22
allele frequency: 1.493347814281835e-3
allele num: 14732
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 9.750390015600624e-4
allele num: 10256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 48
allele frequency: 8.138627962969243e-4
allele num: 58978
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

QD
type: SiteQuality
SIO_000300: 2.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.67e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

DP
type: SiteQuality
SIO_000300: 2.331381e6

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7706
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 2.331381e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.67e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

QD
type: SiteQuality
SIO_000300: 2.84e0

GenotypeQuality
all individuals: 1002
bin: 1.75e1
variant carriers: 34

GenotypeQuality
all individuals: 1474
bin: 2.75e1
variant carriers: 27

GenotypeQuality
all individuals: 964
bin: 1.25e1
variant carriers: 37

GenotypeQuality
all individuals: 2553
bin: 7.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1193
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1815
bin: 2.25e1
variant carriers: 21

GenotypeQuality
all individuals: 3437
bin: 2.5e0
variant carriers: 43

GenotypeQuality
all individuals: 1439
bin: 3.25e1
variant carriers: 23

GenotypeQuality
all individuals: 4966
bin: 9.75e1
variant carriers: 469

GenotypeQuality
all individuals: 6231
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1885
bin: 8.25e1
variant carriers: 13

GenotypeQuality
all individuals: 22190
bin: 6.25e1
variant carriers: 17

GenotypeQuality
all individuals: 2294
bin: 7.25e1
variant carriers: 8

GenotypeQuality
all individuals: 1534
bin: 4.25e1
variant carriers: 19

African
type: Population
allele count: 29
allele frequency: 3.278317883789283e-3
allele num: 8846
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 8.373205741626795e-3
allele num: 836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.959248646927731e-4
allele num: 6282
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.221830029866956e-3
allele num: 14732
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.950078003120125e-3
allele num: 10256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 584
allele frequency: 9.901997354945912e-3
allele num: 58978
num of homozygotes: 1

East Asian
type: Population
allele count: 25
allele frequency: 3.244225279003374e-3
allele num: 7706
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.67e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.331381e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

QD
type: SiteQuality
SIO_000300: 2.84e0

GenotypeQuality
all individuals: 3048
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5159
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66314
num of homozygotes: 0

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

South Asian
type: Population
allele count: 14
allele frequency: 8.485877076009214e-4
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

DP
type: SiteQuality
SIO_000300: 1.855471e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1386
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
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: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

QD
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SIO_000300: 7.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 1.864729e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 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: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 10334
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: 66604
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 6.81e-1

QD
type: SiteQuality
SIO_000300: 9.09e0

VQSLOD
type: SiteQuality
SIO_000300: 2.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

DP
type: SiteQuality
SIO_000300: 1.865875e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.062443164595332e-4
allele num: 6598
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.865626e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.45e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508295263284443e-5
allele num: 66544
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

QD
type: SiteQuality
SIO_000300: 1.554e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

DP
type: SiteQuality
SIO_000300: 1.863284e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeDepth
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 9514
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.859564e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.441e0

VQSLOD
type: SiteQuality
SIO_000300: 6.929999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.99e-1

QD
type: SiteQuality
SIO_000300: 1.139e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.141156867412521e-4
allele num: 8402
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.419e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

QD
type: SiteQuality
SIO_000300: 1.407e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.19e-1

MQRankSum
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SIO_000300: 1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.792186e6

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65760
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.093e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.918e1

QD
type: SiteQuality
SIO_000300: 1.267e1

BaseQRankSum
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SIO_000300: -5.181e0

ClippingRankSum
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SIO_000300: -1.048e0

MQRankSum
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DP
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SIO_000300: 1.791904e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.039698461912578e-5
allele num: 65796
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.439321868520551e-4
allele num: 16398
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

FS
type: SiteQuality
SIO_000300: 4.064e0

QD
type: SiteQuality
SIO_000300: 1.325e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

DP
type: SiteQuality
SIO_000300: 1.791114e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5220700152207e-5
allele num: 65700
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 frequency: 0.0e0
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num of homozygotes: 0

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

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

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65304
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 2
allele frequency: 3.062787136294027e-4
allele num: 6530
num of homozygotes: 0

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 1

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

African
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allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6530
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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65160
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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MQ
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.268713524486171e-4
allele num: 7882
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63328
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11056
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
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SIO_000300: 1.03e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.09e1

VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 1
allele frequency: 1.347345728914039e-4
allele num: 7422
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.61e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 33386
num of homozygotes: 0

European (Finnish)
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South Asian
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Other
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allele num: 466
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Latino
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African
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num of homozygotes: 0

East Asian
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DP
type: SiteQuality
SIO_000300: 7.4735e5

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

South Asian
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European (Non-Finnish)
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num of homozygotes: 0

African
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Latino
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European (Finnish)
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num of homozygotes: 0

Other
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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Other
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DP
type: SiteQuality
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QD
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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ClippingRankSum
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SIO_000300: -4.9e-2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4198
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variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4904
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.630194634402946e-4
allele num: 7604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33788
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.562e0

DP
type: SiteQuality
SIO_000300: 7.77364e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.265e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.45e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.166e0

QD
type: SiteQuality
SIO_000300: 8.31e0

GenotypeQuality
all individuals: 1178
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 4.592422502870264e-4
allele num: 8710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.785028346638898e-5
allele num: 34572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

FS
type: SiteQuality
SIO_000300: 1.1801e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.328e1

DP
type: SiteQuality
SIO_000300: 8.21379e5

VQSLOD
type: SiteQuality
SIO_000300: -3.815e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

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

GenotypeQuality
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GenotypeQuality
all individuals: 1207
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7996
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.682705159048383e-5
allele num: 14964
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.349877e6

MQRankSum
type: SiteQuality
SIO_000300: 6.17e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.97e-1

GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2161
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variant carriers: 1

GenotypeQuality
all individuals: 1227
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61586
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.1441111923921e-5
allele num: 10936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15290
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.383e0

DP
type: SiteQuality
SIO_000300: 1.365643e6

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
SIO_000300: 1.347e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.59e-1

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.59550705214117e-5
allele num: 62676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.814882032667876e-4
allele num: 11020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.384827e6

QD
type: SiteQuality
SIO_000300: 1.323e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1300
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57400994774287e-5
allele num: 63532
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.25675505843911e-4
allele num: 15914
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.653e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545786186854634e-5
allele num: 64692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.645e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
SIO_000300: 3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.115e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.58e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 1.418477e6

GenotypeQuality
all individuals: 70
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 93
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 44892
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64762
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.160670280926565e-5
allele num: 16232
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -1.602e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.754e0

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

QD
type: SiteQuality
SIO_000300: 1.19e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

DP
type: SiteQuality
SIO_000300: 1.420351e6

MQ
type: SiteQuality
SIO_000300: 5.989e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.519064256418047e-5
allele num: 65830
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

QD
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DP
type: SiteQuality
SIO_000300: 1.44036e6

InbreedingCoeff
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SIO_000300: 1.01e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.89e-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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variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512950859356088e-5
allele num: 66096
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -6.204e0

MQ
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SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.445749e6

VQSLOD
type: SiteQuality
SIO_000300: -2.742e-1

FS
type: SiteQuality
SIO_000300: 4.227e0

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1919
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.963864886095837e-4
allele num: 66196
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.75561797752809e-4
allele num: 11392
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.531e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e0

VQSLOD
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SIO_000300: 5.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

DP
type: SiteQuality
SIO_000300: 1.448173e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.01e-2

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
all individuals: 1584
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
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variant carriers: 0

GenotypeQuality
all individuals: 10
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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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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66258
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
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SIO_000300: -2.357e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.559e0

QD
type: SiteQuality
SIO_000300: 6.1e0

DP
type: SiteQuality
SIO_000300: 1.448716e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.86e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017774692941425e-5
allele num: 66274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

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

QD
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SIO_000300: 1.041e1

BaseQRankSum
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SIO_000300: 3.38e0

MQ
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

FS
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MQRankSum
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SIO_000300: -1.019e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.936406995230525e-5
allele num: 10064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66294
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -4.0e-4

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: 9.44e-1

MQ
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SIO_000300: 5.95e1

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508477644361311e-5
allele num: 66292
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.523461304082876e-4
allele num: 6564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.88e-1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
all individuals: 25
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508568670045861e-5
allele num: 66288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.98e-1

DP
type: SiteQuality
SIO_000300: 1.448038e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.269e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 5.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.006e0

QD
type: SiteQuality
SIO_000300: 1.166e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510117789187557e-5
allele num: 66220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.445175e6

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.568e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 4.019e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.353e0

QD
type: SiteQuality
SIO_000300: 8.199999999999999e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.815232722143864e-5
allele num: 11344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65110
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
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ClippingRankSum
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SIO_000300: -2.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

QD
type: SiteQuality
SIO_000300: 1.466e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

DP
type: SiteQuality
SIO_000300: 1.420572e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543448062972681e-5
allele num: 64790
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

DP
type: SiteQuality
SIO_000300: 1.410666e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e0

MQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

QD
type: SiteQuality
SIO_000300: 1.677e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.322556670382757e-4
allele num: 64584
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.536067892503536e-4
allele num: 11312
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.400475e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.717e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64454
num of homozygotes: 0

Latino
type: Population
allele count: 0
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allele num: 11298
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.009e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.391801e6

MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

QD
type: SiteQuality
SIO_000300: 1.395e1

VQSLOD
type: SiteQuality
SIO_000300: 6.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.49e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.552072016141549e-5
allele num: 64430
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Other
type: Population
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele 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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European (Finnish)
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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 count: 5
allele frequency: 7.788161993769471e-5
allele num: 64200
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East Asian
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Other
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

FS
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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MQ
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ClippingRankSum
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SIO_000300: -8.2e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 242
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 4.342162396873643e-4
allele num: 9212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64172
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.467e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-2

FS
type: SiteQuality
SIO_000300: 1.832e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 1.381308e6

QD
type: SiteQuality
SIO_000300: 1.288e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2239
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9190
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.124448799608035e-5
allele num: 16328
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.357e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 1.380569e6

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

FS
type: SiteQuality
SIO_000300: 1.647e0

QD
type: SiteQuality
SIO_000300: 1.004e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11013
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.227897838899803e-4
allele num: 8144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.827e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.591e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.421e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: -1.945e0

DP
type: SiteQuality
SIO_000300: 1.105942e6

GenotypeQuality
all individuals: 9044
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 760
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variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.331203407880724e-4
allele num: 7512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e-1

DP
type: SiteQuality
SIO_000300: 1.268525e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.4e1

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 467
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 89

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2363
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GenotypeQuality
all individuals: 668
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.140105578541875e-4
allele num: 14018
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.997201119552179e-4
allele num: 10004
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

African
type: Population
allele count: 82
allele frequency: 9.369287020109689e-3
allele num: 8752
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55216
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.25e-3
allele num: 800
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.859e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

DP
type: SiteQuality
SIO_000300: 1.293853e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 548
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 855
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GenotypeQuality
all individuals: 2470
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.284026707755521e-4
allele num: 7788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6068
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56030
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14102
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.31534e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.144e1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1487
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6110
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.017543859649122e-5
allele num: 14250
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.337353e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.218e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2523
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.747701772169597e-5
allele num: 57218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.212389380530973e-4
allele num: 9040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.042999999999999e0

MQRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

BaseQRankSum
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.55e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 39943
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GenotypeQuality
all individuals: 467
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59412
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6236
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.079214331966328e-4
allele num: 9266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

FS
type: SiteQuality
SIO_000300: 7.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 6.041e1

MQRankSum
type: SiteQuality
SIO_000300: 8.35e-1

DP
type: SiteQuality
SIO_000300: 1.398973e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

GenotypeQuality
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bin: 7.75e1
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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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626122024196696e-5
allele num: 61496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15098
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.708e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.599e0

DP
type: SiteQuality
SIO_000300: 1.435897e6

MQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2876
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variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.210066769388803e-5
allele num: 62304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.810975609756098e-4
allele num: 10496
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.476e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 1.449768e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

FS
type: SiteQuality
SIO_000300: 1.208e0

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

GenotypeQuality
all individuals: 3713
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.593168493499873e-5
allele num: 62768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15344
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 9.163e0

VQSLOD
type: SiteQuality
SIO_000300: -5.429e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.459208e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.95e0

GenotypeQuality
all individuals: 2985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 45624
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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: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3791
bin: 9.75e1
variant carriers: 83

GenotypeQuality
all individuals: 747
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.359790340696369e-5
allele num: 10684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 82
allele frequency: 1.289146019368633e-3
allele num: 63608
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.024170421958214e-4
allele num: 9764
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.731e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.493e1

DP
type: SiteQuality
SIO_000300: 1.47601e6

GenotypeDepth
all individuals: 101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 2180
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 805
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.34517766497462e-5
allele num: 15760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10848
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.546e1

FS
type: SiteQuality
SIO_000300: 3.403e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.179e0

VQSLOD
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.493585e6

GenotypeQuality
all individuals: 3714
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 3117
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1966
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.75e1
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GenotypeQuality
all individuals: 958
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variant carriers: 0

GenotypeQuality
all individuals: 47274
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15822
num of homozygotes: 0